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Pleurisy
Wikipedia
The Lung Association of Canada explanation of Pleurisy (also available in French) Pleurisy by the American Academy of Family Physicians v t e Symptoms and signs relating to the respiratory system Auscultation Stethoscope Respiratory sounds Stridor Wheeze Crackles Rhonchi Stertor Squawk Pleural friction rub Fremitus Bronchophony Terminal secretions Elicited findings Percussion Pectoriloquy Whispered pectoriloquy Egophony Breathing Rate Apnea Prematurity Dyspnea Hyperventilation Hypoventilation Hyperpnea Tachypnea Hypopnea Bradypnea Pattern Agonal respiration Biot's respiration Cheyne–Stokes respiration Kussmaul breathing Ataxic respiration Other Respiratory distress Respiratory arrest Orthopnea / Platypnea Trepopnea Aerophagia Asphyxia Breath holding Mouth breathing Snoring Other Chest pain In children Precordial catch syndrome Pleurisy Nail clubbing Cyanosis Cough Sputum Hemoptysis Epistaxis Silhouette sign Post-nasal drip Hiccup COPD Hoover's sign asthma Curschmann's spirals Charcot–Leyden crystals chronic bronchitis Reid index sarcoidosis Kveim test pulmonary embolism Hampton hump Westermark sign pulmonary edema Kerley lines Hamman's sign Golden S sign v t e Diseases of the respiratory system Upper RT (including URTIs , common cold ) Head sinuses Sinusitis nose Rhinitis Vasomotor rhinitis Atrophic rhinitis Hay fever Nasal polyp Rhinorrhea nasal septum Nasal septum deviation Nasal septum perforation Nasal septal hematoma tonsil Tonsillitis Adenoid hypertrophy Peritonsillar abscess Neck pharynx Pharyngitis Strep throat Laryngopharyngeal reflux (LPR) Retropharyngeal abscess larynx Croup Laryngomalacia Laryngeal cyst Laryngitis Laryngopharyngeal reflux (LPR) Laryngospasm vocal cords Laryngopharyngeal reflux (LPR) Vocal fold nodule Vocal fold paresis Vocal cord dysfunction epiglottis Epiglottitis trachea Tracheitis Laryngotracheal stenosis Lower RT / lung disease (including LRTIs ) Bronchial / obstructive acute Acute bronchitis chronic COPD Chronic bronchitis Acute exacerbation of COPD ) Asthma ( Status asthmaticus Aspirin-induced Exercise-induced Bronchiectasis Cystic fibrosis unspecified Bronchitis Bronchiolitis Bronchiolitis obliterans Diffuse panbronchiolitis Interstitial / restrictive ( fibrosis ) External agents/ occupational lung disease Pneumoconiosis Aluminosis Asbestosis Baritosis Bauxite fibrosis Berylliosis Caplan's syndrome Chalicosis Coalworker's pneumoconiosis Siderosis Silicosis Talcosis Byssinosis Hypersensitivity pneumonitis Bagassosis Bird fancier's lung Farmer's lung Lycoperdonosis Other ARDS Combined pulmonary fibrosis and emphysema Pulmonary edema Löffler's syndrome / Eosinophilic pneumonia Respiratory hypersensitivity Allergic bronchopulmonary aspergillosis Hamman-Rich syndrome Idiopathic pulmonary fibrosis Sarcoidosis Vaping-associated pulmonary injury Obstructive / Restrictive Pneumonia / pneumonitis By pathogen Viral Bacterial Pneumococcal Klebsiella Atypical bacterial Mycoplasma Legionnaires' disease Chlamydiae Fungal Pneumocystis Parasitic noninfectious Chemical / Mendelson's syndrome Aspiration / Lipid By vector/route Community-acquired Healthcare-associated Hospital-acquired By distribution Broncho- Lobar IIP UIP DIP BOOP-COP NSIP RB Other Atelectasis circulatory Pulmonary hypertension Pulmonary embolism Lung abscess Pleural cavity / mediastinum Pleural disease Pleuritis/pleurisy Pneumothorax / Hemopneumothorax Pleural effusion Hemothorax Hydrothorax Chylothorax Empyema/pyothorax Malignant Fibrothorax Mediastinal disease Mediastinitis Mediastinal emphysema Other/general Respiratory failure Influenza Common cold SARS Coronavirus disease 2019 Idiopathic pulmonary haemosiderosis Pulmonary alveolar proteinosis Authority control NDL : 00569657IL10, TNF, IL1B, ICAM1, IL6, SELP, MEFV, PRTN3, DNAH11, HLA-DPA1, IL12A, KLRC4, STAT4, TREX1, PTPN22, TLR4, ERAP1, HLA-DPB1, TNFRSF1A, HLA-B, NOD2, IL12A-AS1, FAS, FCGR2B, C4A, FCGR2A, UBAC2, IL23R, DNASE1, CCR1, CTLA4, CCL2, NFE2L2, MPO, ADA, TLR9, GABPA, TIMELESS, HAVCR1, MIR210, TP53, TPI1, WNT3, NOX4, ARHGEF5, KEAP1, TNFRSF1B, SIRT1, BAP1, PLA2G10, INTS4, NLRP3, SH2B2, RBM45, PLA2G2A, TRBV20OR9-2, IFNA13, AGTR1, KLK3, CD4, CDKN2A, CCR4, CYP1A1, ESAT, CXCR3, HLA-DRB1, HMOX1, IFNA1, IFNG, STAT3, IL2, IL4, IL17A, LAG3, STMN1, MTAP, PIK3CG, AGT, RORC, RPS19, SSB, H3P10
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Visual Agnosia
Wikipedia
See also [ edit ] Agnosia Blindness Color agnosia Gestaltzerfall Prosopagnosia Riddoch syndrome Topographical disorientation References [ edit ] ^ Delver, J. ... OCLC 57182718 . v t e Optical illusions ( list ) Illusions Afterimage Ambiguous image Ames room Barberpole Bezold Café wall Checker shadow Chubb Cornsweet Delboeuf Ebbinghaus Ehrenstein Flash lag Fraser spiral Gravity hill Grid Hering Impossible trident Jastrow Lilac chaser Mach bands McCollough Müller-Lyer Necker cube Orbison Penrose stairs Penrose triangle Peripheral drift Poggendorff Ponzo Rubin vase Sander Schroeder stairs Shepard tables Spinning Dancer Ternus Vertical–horizontal White's Wundt Zöllner Popular culture Op art Trompe-l'œil Spectropia (1864 book) Ascending and Descending (1960 drawing) Waterfall (1961 drawing) The dress (2015 photograph) Related Accidental viewpoint Auditory illusions Tactile illusions Temporal illusion v t e Sensation and perception Processes and concepts Sensation Stimulus Sensory receptor Transduction (physiology) Sensory processing Active sensory system Perception Multimodal integration Awareness Consciousness Cognition Feeling Qualia Human External Sensory organs Eyes Ears Inner ear Nose Mouth Skin Sensory systems Visual system (sense of vision) Auditory system (sense of hearing) Vestibular system (sense of balance) Olfactory system (sense of smell) Gustatory system (sense of taste) Somatosensory system (sense of touch) Sensory cranial and spinal nerves Optic (II) Vestibulocochlear (VIII) Olfactory (I) Facial (VII) Glossopharyngeal (IX) Trigeminal (V) Spinal Cerebral cortices Visual cortex Auditory cortex Vestibular cortex Olfactory cortex Gustatory cortex Somatosensory cortex Perceptions Visual perception (vision) Auditory perception (hearing) Equilibrioception (balance) Olfaction (smell) Gustation (taste or flavor) Touch mechanoreception nociception (pain) thermoception Internal Proprioception Hunger Thirst Suffocation Nausea Nonhuman Animal Electroception Magnetoreception Echolocation Infrared sensing in vampire bats Infrared sensing in snakes Surface wave detection Frog hearing Toad vision Plant Photomorphogenesis Gravitropism Artificial Robotic sensing Computer vision Machine hearing Types of sensory receptors Mechanoreceptor Baroreceptor Mechanotransduction Lamellar corpuscle Tactile corpuscle Merkel nerve ending Bulbous corpuscle Campaniform sensilla Slit sensilla Stretch receptor Photoreceptor Photoreceptor cell Cone cell Rod cell ipRGC Photopigment Aureochrome Chemoreceptor Taste receptor Olfactory receptor Osmoreceptor Thermoreceptor Cilium TRP channels Nociceptor Nociceptin receptor Juxtacapillary receptor Disorders Visual Visual impairment Alice in Wonderland syndrome Amaurosis Anopsia Color blindness Diplopia Hemeralopia and Nyctalopia Optic neuropathy Oscillopsia Palinopsia Papilledema Photophobia Photopsia Polyopia Scotoma Stereoblindness Visual snow Auditory Amblyaudia Auditory agnosia Auditory hallucination Auditory verbal agnosia Cortical deafness Hearing loss Microwave auditory effect Music-specific disorders Palinopsia Spatial hearing loss Tinnitus Vestibular Vertigo BPPV Labyrinthine fistula Labyrinthitis Ménière's disease Olfactory Anosmia Dysosmia Hyperosmia Hyposmia Olfactory reference syndrome Parosmia Phantosmia Gustatory Ageusia Hypergeusia Hypogeusia Parageusia Tactile Astereognosis CMT disease Formication Hyperesthesia Hypoesthesia Paresthesia Tactile hallucination Nociception (pain) Hyperalgesia Hypoalgesia Pain dissociation Phantom pain Proprioception Asomatognosia Phantom limb syndrome Somatoparaphrenia Supernumerary phantom limb Multimodal Aura Agnosia Allochiria Derealization Hallucination HSAN Pareidolia Sensory processing disorder Synesthesia v t e Phenomena of the visual system Entoptic phenomena Blind spot Phosphene Floater Afterimage Haidinger's brush Prisoner's cinema Blue field entoptic phenomenon Purkinje images Other phenomena Aura Form constant Scintillating scotoma Palinopsia Visual snow Afterimage on empty shape Cosmic ray visual phenomena Scotopic sensitivity syndrome Closed-eye hallucination
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Rift Valley Fever
Wikipedia
Human viral disease Rift Valley fever TEM micrograph of tissue infected with Rift Valley fever virus Specialty Infectious disease Symptoms Fever , muscle pains , headaches [1] Complications Loss of sight, confusion , bleeding, liver problems [1] Duration Up to a week [1] Causes Phlebovirus spread by an infected animal or mosquito [1] Diagnostic method Finding antibodies or the virus in the blood [1] Prevention Vaccinating animals against the disease, decreasing mosquito bites [1] Treatment Supportive care [1] Frequency Outbreaks in Africa and Arabia [1] Rift Valley fever ( RVF ) is a viral disease of humans and livestock that can cause mild to severe symptoms. [1] The mild symptoms may include: fever , muscle pains , and headaches which often last for up to a week. [1] The severe symptoms may include: loss of sight beginning three weeks after the infection, infections of the brain causing severe headaches and confusion , and bleeding together with liver problems which may occur within the first few days. [1] Those who have bleeding have a chance of death as high as 50%. [1] The disease is caused by the RVF virus , which is of the Phlebovirus type. [1] It is spread by either touching infected animal blood, breathing in the air around an infected animal being butchered , drinking raw milk from an infected animal, or the bite of infected mosquitoes . [1] Animals such as cows, sheep, goats, and camels may be affected. [1] In these animals it is spread mostly by mosquitoes. [1] It does not appear that one person can infect another person. [1] The disease is diagnosed by finding antibodies against the virus or the virus itself in the blood. [1] Prevention of the disease in humans is accomplished by vaccinating animals against the disease. [1] This must be done before an outbreak occurs because if it is done during an outbreak it may worsen the situation. [1] Stopping the movement of animals during an outbreak may also be useful, as may decreasing mosquito numbers and avoiding their bites. [1] There is a human vaccine ; however, as of 2010 it is not widely available. [1] There is no specific treatment and medical efforts are supportive. [1] Outbreaks of the disease have only occurred in Africa and Arabia . [1] Outbreaks usually occur during periods of increased rain which increase the number of mosquitoes. [1] The disease was first reported among livestock in Rift Valley of Kenya in the early 1900s, [2] and the virus was first isolated in 1931. [1] Contents 1 Signs and symptoms 2 Cause 2.1 Virology 2.2 Transmission 3 Pathogenesis 4 Diagnosis 5 Prevention 6 Epidemiology 7 Biological weapon 8 Research 9 See also 10 References 11 External links Signs and symptoms [ edit ] In humans, the virus can cause several syndromes. Usually, sufferers have either no symptoms or only a mild illness with fever, headache , muscle pains , and liver abnormalities. In a small percentage of cases (< 2%), the illness can progress to hemorrhagic fever syndrome, meningoencephalitis (inflammation of the brain and tissues lining the brain ), or affect the eye. ... Classification D ICD - 10 : A92.4 ICD - 9-CM : 066.3 MeSH : D012295 DiseasesDB : 31094 External resources Orphanet : 319251 v t e Zoonotic viral diseases (A80–B34, 042–079 ) Arthropod -borne Mosquito -borne Bunyavirales Arbovirus encephalitides : La Crosse encephalitis LACV Batai virus BATV Bwamba Fever BWAV California encephalitis CEV Jamestown Canyon encephalitis Tete virus Tahyna virus TAHV Viral hemorrhagic fevers : Rift Valley fever RVFV Bunyamwera fever BUNV Ngari virus NRIV Flaviviridae Arbovirus encephalitides : Japanese encephalitis JEV Australian encephalitis MVEV KUNV Saint Louis encephalitis SLEV Usutu virus West Nile fever WNV Viral hemorrhagic fevers : Dengue fever DENV-1-4 Yellow fever YFV Zika fever Zika virus Togaviridae Arbovirus encephalitides : Eastern equine encephalomyelitis EEEV Western equine encephalomyelitis WEEV Venezuelan equine encephalomyelitis VEEV Chikungunya CHIKV O'nyong'nyong fever ONNV Pogosta disease Sindbis virus Ross River fever RRV Semliki Forest virus Reoviridae Banna virus encephalitis Tick -borne Bunyavirales Viral hemorrhagic fevers : Bhanja virus Crimean–Congo hemorrhagic fever (CCHFV) Heartland virus Severe fever with thrombocytopenia syndrome ( Huaiyangshan banyangvirus ) Tete virus Flaviviridae Arbovirus encephalitides : Tick-borne encephalitis TBEV Powassan encephalitis POWV Viral hemorrhagic fevers : Omsk hemorrhagic fever OHFV Kyasanur Forest disease KFDV AHFV Langat virus LGTV Orthomyxoviridae Bourbon virus Reoviridae Colorado tick fever CTFV Kemerovo tickborne viral fever Sandfly -borne Bunyavirales Adria virus (ADRV) Oropouche fever Oropouche virus Pappataci fever Toscana virus Sandfly fever Naples virus Rhabdoviridae Chandipura virus Mammal -borne Rodent -borne Arenaviridae Viral hemorrhagic fevers : Lassa fever LASV Venezuelan hemorrhagic fever GTOV Argentine hemorrhagic fever JUNV Brazilian hemorrhagic fever SABV Bolivian hemorrhagic fever MACV LUJV CHPV Bunyavirales Hemorrhagic fever with renal syndrome DOBV HTNV PUUV SEOV AMRV THAIV Hantavirus pulmonary syndrome ANDV SNV Herpesviridae Murid gammaherpesvirus 4 Bat -borne Filoviridae BDBV SUDV TAFV Marburg virus disease MARV RAVV Rhabdoviridae Rabies ABLV MOKV DUVV LBV CHPV Paramyxoviridae Henipavirus encephalitis HeV NiV Coronaviridae SARS-related coronavirus SARS-CoV MERS-CoV SARS-CoV-2 Primate -borne Herpesviridae Macacine alphaherpesvirus 1 Retroviridae Simian foamy virus HTLV-1 HTLV-2 Poxviridae Tanapox Yaba monkey tumor virus Multiple vectors Rhabdoviridae Rabies RABV Mokola virus Poxviridae Monkeypox Taxon identifiers Wikidata : Q14276794 Wikispecies : Rift Valley fever phlebovirus IRMNG : 11460687 ISC : 66184 NCBI : 11588GTF2H2, XRN1, CD83, GRAP2, AHSA1, KHDRBS1, NUP62, RNF19A, POLDIP2, FBXO3, DCTN4, ACTB, AIMP2, POLE4, POLD4, UBASH3B, NLRP3, NUDT16, TRIM69, TICAM1, GTF2H5, LINC00273, SQSTM1, TNF, ANXA6, GTF2H1, CD40LG, CRK, MAPK14, CTNNB1, EIF4EBP1, EIF4G1, ERCC2, ERCC3, GTF2H3, THOP1, GTF2H4, IFNA2, IFNAR1, IL1B, NUP98, MAPK1, STAT3, TERT, H3P5
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Cat-Scratch Disease
Wikipedia
In rare situations, CSD can lead to the development of serious neurologic or cardiac sequelae such as meningoencephalitis , encephalopathy , seizures , or endocarditis . [4] Endocarditis associated with Bartonella infection has a particularly high mortality. [5] Parinaud's oculoglandular syndrome is the most common ocular manifestation of CSD, [4] and is a granulomatous conjunctivitis with concurrent swelling of the lymph node near the ear. [6] Optic neuritis or neuroretinitis is one of the atypical presentations. [7] People who are immunocompromised are susceptible to other conditions associated with B. henselae and B. quintana , such as bacillary angiomatosis or bacillary peliosis . [4] Bacillary angiomatosis is primarily a vascular skin lesion that may extend to bone or be present in other areas of the body. ... Pathologists believe that the increased incidence of CSD is due to cat owners neglecting to vaccinate their cats. [23] History [ edit ] Symptoms similar to CSD were first described by Henri Parinaud in 1889, and the clinical syndrome was first described in 1950 by Robert Debré . [24] [5] In 1983, the Warthin-Starry silver stain was used to discover a Gram-negative bacillus which was named Afipia felis in 1991 after it was successfully cultured and isolated. ... External links [ edit ] Classification D ICD - 10 : A28.1 ICD - 9-CM : 078.3 MeSH : D002372 DiseasesDB : 2173 External resources MedlinePlus : 001614 eMedicine : emerg/84 Patient UK : Cat-scratch disease https://www.cdc.gov/bartonella/cat-scratch/index.html DermNet bacterial/catscratch Cat Scratch Disease on National Organization for Rare Disorders site v t e Domestic cats Felinology Anatomy Genetics Dwarf cat Kitten Odd-eyed cat Squitten Coat genetics Bicolor cat Black cat Calico cat Tabby cat Tortoiseshell cat Health Aging Declawing Diet dental health senior Neutering Spaying Vaccination Behavior Body language Catfight Catnip valerian Communication Meow Purr Kneading Intelligence Play and toys Righting reflex Senses Human–cat interaction Ailurophobia Animal-assisted therapy Bodega cat Cat cafés Cat massage Cat meat Cat-scratch disease Cat show Cats in ancient Egypt Cultural depictions Internet Farm cat Feral cat Cats and Islam Lolcat National Cat Day Puppy cat Ship's cat Zoonosis Registries American Cat Fanciers Association Associazione Nazionale Felina Italiana Canadian Cat Association Cat Aficionado Association Cat Fanciers' Association Fédération Internationale Féline Governing Council of the Cat Fancy Southern Africa Cat Council The International Cat Association World Cat Congress World Cat Federation Breeds ( full list ) ( experimental ) Fully domestic Abyssinian American Curl American Shorthair Balinese Brazilian Shorthair British Shorthair Birman Bombay Burmese Burmilla California Spangled Chartreux Chinese Li Hua Colorpoint Shorthair Cornish Rex Cymric Devon Rex Donskoy Egyptian Mau European Shorthair Exotic Shorthair German Rex Himalayan Japanese Bobtail Javanese Khao Manee Korat Kurilian Bobtail Lykoi Maine Coon Manx Munchkin Norwegian Forest Ocicat Ojos Azules Oriental Shorthair Persian Peterbald Pixie-bob Raas Ragdoll Ragamuffin Russian Blue Scottish Fold Selkirk Rex Siamese Siberian Singapura Snowshoe Somali Sphynx Thai Traditional Persian Tonkinese Toyger Turkish Angora Turkish Van Hybrid Bengal Chausie Highlander Savannah Serengeti Landraces Aegean Cyprus Domestic long-haired Domestic short-haired Kellas Sokoke Van Diseases and disorders Acne Asthma Calicivirus Congenital sensorineural deafness Feline corneal sequestrum Flea Heartworm Hepatic lipidosis Hypertrophic cardiomyopathy Immunodeficiency virus Infectious peritonitis Leukemia virus Lower urinary tract disease Panleukopenia Polydactyly Rabies Ringworm Roundworm Skin disorders Tick Toxoplasmosis Viral rhinotracheitis Book Category v t e Proteobacteria -associated Gram-negative bacterial infections α Rickettsiales Rickettsiaceae / ( Rickettsioses ) Typhus Rickettsia typhi Murine typhus Rickettsia prowazekii Epidemic typhus , Brill–Zinsser disease , Flying squirrel typhus Spotted fever Tick-borne Rickettsia rickettsii Rocky Mountain spotted fever Rickettsia conorii Boutonneuse fever Rickettsia japonica Japanese spotted fever Rickettsia sibirica North Asian tick typhus Rickettsia australis Queensland tick typhus Rickettsia honei Flinders Island spotted fever Rickettsia africae African tick bite fever Rickettsia parkeri American tick bite fever Rickettsia aeschlimannii Rickettsia aeschlimannii infection Mite-borne Rickettsia akari Rickettsialpox Orientia tsutsugamushi Scrub typhus Flea-borne Rickettsia felis Flea-borne spotted fever Anaplasmataceae Ehrlichiosis : Anaplasma phagocytophilum Human granulocytic anaplasmosis , Anaplasmosis Ehrlichia chaffeensis Human monocytotropic ehrlichiosis Ehrlichia ewingii Ehrlichiosis ewingii infection Rhizobiales Brucellaceae Brucella abortus Brucellosis Bartonellaceae Bartonellosis : Bartonella henselae Cat-scratch disease Bartonella quintana Trench fever Either B. henselae or B. quintana Bacillary angiomatosis Bartonella bacilliformis Carrion's disease , Verruga peruana β Neisseriales M+ Neisseria meningitidis/meningococcus Meningococcal disease , Waterhouse–Friderichsen syndrome , Meningococcal septicaemia M− Neisseria gonorrhoeae/gonococcus Gonorrhea ungrouped: Eikenella corrodens / Kingella kingae HACEK Chromobacterium violaceum Chromobacteriosis infection Burkholderiales Burkholderia pseudomallei Melioidosis Burkholderia mallei Glanders Burkholderia cepacia complex Bordetella pertussis / Bordetella parapertussis Pertussis γ Enterobacteriales ( OX− ) Lac+ Klebsiella pneumoniae Rhinoscleroma , Pneumonia Klebsiella granulomatis Granuloma inguinale Klebsiella oxytoca Escherichia coli : Enterotoxigenic Enteroinvasive Enterohemorrhagic O157:H7 O104:H4 Hemolytic-uremic syndrome Enterobacter aerogenes / Enterobacter cloacae Slow/weak Serratia marcescens Serratia infection Citrobacter koseri / Citrobacter freundii Lac− H2S+ Salmonella enterica Typhoid fever , Paratyphoid fever , Salmonellosis H2S− Shigella dysenteriae / sonnei / flexneri / boydii Shigellosis , Bacillary dysentery Proteus mirabilis / Proteus vulgaris Yersinia pestis Plague / Bubonic plague Yersinia enterocolitica Yersiniosis Yersinia pseudotuberculosis Far East scarlet-like fever Pasteurellales Haemophilus : H. influenzae Haemophilus meningitis Brazilian purpuric fever H. ducreyi Chancroid H. parainfluenzae HACEK Pasteurella multocida Pasteurellosis Actinobacillus Actinobacillosis Aggregatibacter actinomycetemcomitans HACEK Legionellales Legionella pneumophila / Legionella longbeachae Legionnaires' disease Coxiella burnetii Q fever Thiotrichales Francisella tularensis Tularemia Vibrionaceae Vibrio cholerae Cholera Vibrio vulnificus Vibrio parahaemolyticus Vibrio alginolyticus Plesiomonas shigelloides Pseudomonadales Pseudomonas aeruginosa Pseudomonas infection Moraxella catarrhalis Acinetobacter baumannii Xanthomonadaceae Stenotrophomonas maltophilia Cardiobacteriaceae Cardiobacterium hominis HACEK Aeromonadales Aeromonas hydrophila / Aeromonas veronii Aeromonas infection ε Campylobacterales Campylobacter jejuni Campylobacteriosis , Guillain–Barré syndrome Helicobacter pylori Peptic ulcer , MALT lymphoma , Gastric cancer Helicobacter cinaedi Helicobacter cellulitis
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Human Parainfluenza Viruses
Wikipedia
By the age of 10, the majority of children are sero-positive for HPIV-4 infection which may be indicative of a large proportion of asymptomatic or mild infections. [3] Important epidemiological factors that are associated with a higher risk of infection and mortality are those who are immuno-compromised and may be taken ill with more extreme forms of LRI. [13] Associations between HPIVs and neurologic disease are known; for example, hospitalisation with certain HPIVs has a strong association with febrile seizures . [23] HPIV-4B has the strongest association (up to 62%) followed by hPIV-3 and -1. [3] HPIVs have also been linked with rare cases of virally caused meningitis [24] and Guillain–Barré syndrome . [12] HPIVs are spread from person to person ('horizontal transmission') by contact with infected secretions through respiratory droplets or contaminated surfaces or objects. ... Human Parainfluenza Viruses (HPIVs) External links [ edit ] Human Parainfluenza Viruses – information provided by the CDC Classification D ICD - 10 : B34.8 , J12.2 , J20.4 ICD - 9-CM : 480.2 MeSH : D018184 DiseasesDB : 30631 External resources MedlinePlus : 001370 v t e Infectious diseases – viral systemic diseases Oncovirus DNA virus HBV Hepatocellular carcinoma HPV Cervical cancer Anal cancer Penile cancer Vulvar cancer Vaginal cancer Oropharyngeal cancer KSHV Kaposi's sarcoma EBV Nasopharyngeal carcinoma Burkitt's lymphoma Hodgkin lymphoma Follicular dendritic cell sarcoma Extranodal NK/T-cell lymphoma, nasal type MCPyV Merkel-cell carcinoma RNA virus HCV Hepatocellular carcinoma Splenic marginal zone lymphoma HTLV-I Adult T-cell leukemia/lymphoma Immune disorders HIV AIDS Central nervous system Encephalitis / meningitis DNA virus Human polyomavirus 2 Progressive multifocal leukoencephalopathy RNA virus MeV Subacute sclerosing panencephalitis LCV Lymphocytic choriomeningitis Arbovirus encephalitis Orthomyxoviridae (probable) Encephalitis lethargica RV Rabies Chandipura vesiculovirus Herpesviral meningitis Ramsay Hunt syndrome type 2 Myelitis Poliovirus Poliomyelitis Post-polio syndrome HTLV-I Tropical spastic paraparesis Eye Cytomegalovirus Cytomegalovirus retinitis HSV Herpes of the eye Cardiovascular CBV Pericarditis Myocarditis Respiratory system / acute viral nasopharyngitis / viral pneumonia DNA virus Epstein–Barr virus EBV infection / Infectious mononucleosis Cytomegalovirus RNA virus IV : Human coronavirus 229E / NL63 / HKU1 / OC43 Common cold MERS coronavirus Middle East respiratory syndrome SARS coronavirus Severe acute respiratory syndrome SARS coronavirus 2 Coronavirus disease 2019 V , Orthomyxoviridae : Influenza virus A / B / C / D Influenza / Avian influenza V, Paramyxoviridae : Human parainfluenza viruses Parainfluenza Human orthopneumovirus hMPV Human digestive system Pharynx / Esophagus MuV Mumps Cytomegalovirus Cytomegalovirus esophagitis Gastroenteritis / diarrhea DNA virus Adenovirus Adenovirus infection RNA virus Rotavirus Norovirus Astrovirus Coronavirus Hepatitis DNA virus HBV ( B ) RNA virus CBV HAV ( A ) HCV ( C ) HDV ( D ) HEV ( E ) HGV ( G ) Pancreatitis CBV Urogenital BK virus MuV Mumps v t e Common cold Viruses Adenovirus Coronavirus Enterovirus Rhinovirus Symptoms Cough Fatigue Fever Headache Loss of appetite Malaise Muscle aches Nasal congestion Rhinorrhea Sneezing Sore throat Weakness Complications Acute bronchitis Bronchiolitis Croup Otitis media Pharyngitis Pneumonia Sinusitis Strep throat Drugs Antiviral drugs Pleconaril (experimental)
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Anal Cancer
Wikipedia
External links [ edit ] Classification D ICD - 10 : C21 MeSH : D001005 DiseasesDB : 31467 External resources NCI : Anal cancer American Cancer Society: Anal Cancer Anal cancer information from Cancer Research UK National Cancer Institute: Anal cancer v t e Digestive system neoplasia GI tract Upper Esophagus Squamous cell carcinoma Adenocarcinoma Stomach Gastric carcinoma Signet ring cell carcinoma Gastric lymphoma MALT lymphoma Linitis plastica Lower Small intestine Duodenal cancer Adenocarcinoma Appendix Carcinoid Pseudomyxoma peritonei Colon/rectum Colorectal polyp : adenoma , hyperplastic , juvenile , sessile serrated adenoma , traditional serrated adenoma , Peutz–Jeghers Cronkhite–Canada Polyposis syndromes: Juvenile MUTYH-associated Familial adenomatous / Gardner's Polymerase proofreading-associated Serrated polyposis Neoplasm: Adenocarcinoma Familial adenomatous polyposis Hereditary nonpolyposis colorectal cancer Anus Squamous cell carcinoma Upper and/or lower Gastrointestinal stromal tumor Krukenberg tumor (metastatic) Accessory Liver malignant : Hepatocellular carcinoma Fibrolamellar Hepatoblastoma benign : Hepatocellular adenoma Cavernous hemangioma hyperplasia : Focal nodular hyperplasia Nodular regenerative hyperplasia Biliary tract bile duct : Cholangiocarcinoma Klatskin tumor gallbladder : Gallbladder cancer Pancreas exocrine pancreas : Adenocarcinoma Pancreatic ductal carcinoma cystic neoplasms : Serous microcystic adenoma Intraductal papillary mucinous neoplasm Mucinous cystic neoplasm Solid pseudopapillary neoplasm Pancreatoblastoma Peritoneum Primary peritoneal carcinoma Peritoneal mesothelioma Desmoplastic small round cell tumor v t e Infectious diseases – viral systemic diseases Oncovirus DNA virus HBV Hepatocellular carcinoma HPV Cervical cancer Anal cancer Penile cancer Vulvar cancer Vaginal cancer Oropharyngeal cancer KSHV Kaposi's sarcoma EBV Nasopharyngeal carcinoma Burkitt's lymphoma Hodgkin lymphoma Follicular dendritic cell sarcoma Extranodal NK/T-cell lymphoma, nasal type MCPyV Merkel-cell carcinoma RNA virus HCV Hepatocellular carcinoma Splenic marginal zone lymphoma HTLV-I Adult T-cell leukemia/lymphoma Immune disorders HIV AIDS Central nervous system Encephalitis / meningitis DNA virus Human polyomavirus 2 Progressive multifocal leukoencephalopathy RNA virus MeV Subacute sclerosing panencephalitis LCV Lymphocytic choriomeningitis Arbovirus encephalitis Orthomyxoviridae (probable) Encephalitis lethargica RV Rabies Chandipura vesiculovirus Herpesviral meningitis Ramsay Hunt syndrome type 2 Myelitis Poliovirus Poliomyelitis Post-polio syndrome HTLV-I Tropical spastic paraparesis Eye Cytomegalovirus Cytomegalovirus retinitis HSV Herpes of the eye Cardiovascular CBV Pericarditis Myocarditis Respiratory system / acute viral nasopharyngitis / viral pneumonia DNA virus Epstein–Barr virus EBV infection / Infectious mononucleosis Cytomegalovirus RNA virus IV : Human coronavirus 229E / NL63 / HKU1 / OC43 Common cold MERS coronavirus Middle East respiratory syndrome SARS coronavirus Severe acute respiratory syndrome SARS coronavirus 2 Coronavirus disease 2019 V , Orthomyxoviridae : Influenza virus A / B / C / D Influenza / Avian influenza V, Paramyxoviridae : Human parainfluenza viruses Parainfluenza Human orthopneumovirus hMPV Human digestive system Pharynx / Esophagus MuV Mumps Cytomegalovirus Cytomegalovirus esophagitis Gastroenteritis / diarrhea DNA virus Adenovirus Adenovirus infection RNA virus Rotavirus Norovirus Astrovirus Coronavirus Hepatitis DNA virus HBV ( B ) RNA virus CBV HAV ( A ) HCV ( C ) HDV ( D ) HEV ( E ) HGV ( G ) Pancreatitis CBV Urogenital BK virus MuV Mumps v t e Human papillomavirus Related diseases Cancers Cervical cancer cancers Anal Vaginal Vulvar Penile Head and neck cancer ( HPV-positive oropharyngeal cancer ) Warts genital plantar flat Laryngeal papillomatosis Epidermodysplasia verruciformis Focal epithelial hyperplasia Papilloma Others Acrochordon ( skin tags ) Vaccine HPV vaccines Cervarix Gardasil Screening Pap test : stain Bethesda system Cytopathology Cytotechnology Experimental techniques: Speculoscopy Cervicography Colposcopy Biopsy histology Cervical intraepithelial neoplasia (CIN) Koilocyte Vaginal intraepithelial neoplasia (VAIN) Vulvar intraepithelial neoplasia (VIN) Treatment Cervical conization Loop electrical excision procedure (LEEP) History Georgios Papanikolaou Harald zur Hausen v t e Sexually transmitted infections (STI) Bacterial Chancroid ( Haemophilus ducreyi ) Chlamydia , lymphogranuloma venereum ( Chlamydia trachomatis ) Donovanosis ( Klebsiella granulomatis ) Gonorrhea ( Neisseria gonorrhoeae ) Mycoplasma hominis infection ( Mycoplasma hominis ) Syphilis ( Treponema pallidum ) Ureaplasma infection ( Ureaplasma urealyticum ) Protozoal Trichomoniasis ( Trichomonas vaginalis ) Parasitic Crab louse Scabies Viral AIDS ( HIV-1/HIV-2 ) Cancer cervical vulvar penile anal Human papillomavirus (HPV) Genital warts ( condyloma ) Hepatitis B ( Hepatitis B virus ) Herpes simplex HSV-1 & HSV-2 Molluscum contagiosum ( MCV ) General inflammation female Cervicitis Pelvic inflammatory disease (PID) male Epididymitis Prostatitis either Proctitis Urethritis / Non-gonococcal urethritis (NGU)
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Bcl11a-Related Intellectual Disability
Gene_reviews
Includes partial or whole-gene deletions of BCL11A without disrupting other protein-coding genes (excludes contiguous gene deletion syndromes, namely 2p15-16.1 microdeletion syndrome). 9. ... See OMIM Phenotypic Series: Autosomal dominant ID, Autosomal recessive ID, Nonsyndromic X-linked ID, and Syndromic X-linked ID. Table 2. Selected Disorders to Consider in the Differential Diagnosis of BCL11A -Related Intellectual Disability View in own window Disorder Gene(s) MOI Key Clinical Features of Differential Diagnosis Disorder Overlapping w/ BCL11A -ID Distinguishing from BCL11A -ID KANSL1 -related intellectual disability syndrome KANSL1 AD ID, infant hypotonia, joint hypermobility, everted lower lip, strabismus Facial features incl blepharophimosis & bulbous or tubular nose More frequent congenital anomalies (renal & urogenital anomalies, heart defects) Alpha-thalassemia X-linked intellectual disability syndrome (ATRX) ATRX XL ID, hypotonia, small head circumference, everted lower lip, short nose, short stature Facial gestalt in a subset of individuals w/ BCL11A -ID resembles that of ATRX. 1 Craniofacial features (telecanthus, tented vermilion of upper lip, progressive coarsening of facial features), genital abnormalities, & skeletal abnormalities ID is typically severe to profound in boys (heterozygous females w/craniofacial features, ID, & growth restriction have been described). 2 Alpha-thalassemia (in ~85% of individuals) AD = autosomal dominant; ID = intellectual disability; MOI = mode of inheritance; XL = X-linked 1.
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Maple Syrup Urine Disease
Wikipedia
External links [ edit ] Classification D ICD - 10 : E71.0 ICD - 9-CM : 270.3 OMIM : 248600 MeSH : D008375 DiseasesDB : 7820 External resources MedlinePlus : 000373 eMedicine : ped/1368 Patient UK : Maple syrup urine disease GeneReviews : Maple Syrup Urine Disease Orphanet : 511 Maple syrup urine disease at NLM Genetics Home Reference msud at NIH / UW GeneTests v t e Inborn error of amino acid metabolism K → acetyl-CoA Lysine /straight chain Glutaric acidemia type 1 type 2 Hyperlysinemia Pipecolic acidemia Saccharopinuria Leucine 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency 3-Methylglutaconic aciduria 1 Isovaleric acidemia Maple syrup urine disease Tryptophan Hypertryptophanemia G G→ pyruvate → citrate Glycine D-Glyceric acidemia Glutathione synthetase deficiency Sarcosinemia Glycine → Creatine : GAMT deficiency Glycine encephalopathy G→ glutamate → α-ketoglutarate Histidine Carnosinemia Histidinemia Urocanic aciduria Proline Hyperprolinemia Prolidase deficiency Glutamate / glutamine SSADHD G→ propionyl-CoA → succinyl-CoA Valine Hypervalinemia Isobutyryl-CoA dehydrogenase deficiency Maple syrup urine disease Isoleucine 2-Methylbutyryl-CoA dehydrogenase deficiency Beta-ketothiolase deficiency Maple syrup urine disease Methionine Cystathioninuria Homocystinuria Hypermethioninemia General BC / OA Methylmalonic acidemia Methylmalonyl-CoA mutase deficiency Propionic acidemia G→ fumarate Phenylalanine / tyrosine Phenylketonuria 6-Pyruvoyltetrahydropterin synthase deficiency Tetrahydrobiopterin deficiency Tyrosinemia Alkaptonuria / Ochronosis Tyrosinemia type I Tyrosinemia type II Tyrosinemia type III / Hawkinsinuria Tyrosine → Melanin Albinism : Ocular albinism ( 1 ) Oculocutaneous albinism ( Hermansky–Pudlak syndrome ) Waardenburg syndrome Tyrosine → Norepinephrine Dopamine beta hydroxylase deficiency reverse: Brunner syndrome G→ oxaloacetate Urea cycle / Hyperammonemia ( arginine aspartate ) Argininemia Argininosuccinic aciduria Carbamoyl phosphate synthetase I deficiency Citrullinemia N-Acetylglutamate synthase deficiency Ornithine transcarbamylase deficiency / translocase deficiency Transport / IE of RTT Solute carrier family : Cystinuria Hartnup disease Iminoglycinuria Lysinuric protein intolerance Fanconi syndrome : Oculocerebrorenal syndrome Cystinosis Other 2-Hydroxyglutaric aciduria Aminoacylase 1 deficiency Ethylmalonic encephalopathy Fumarase deficiency Trimethylaminuria Authority control GND : 4217419-3
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Heart Attack
Mayo_clinic
High blood sugar increases the risk of a heart attack. Metabolic syndrome. This is a combination of at least three of the following things: enlarged waist (central obesity), high blood pressure, low good cholesterol, high triglycerides and high blood sugar. Having metabolic syndrome makes you twice as likely to develop heart disease than if you don't have it. ... This condition may be called Dressler syndrome, postmyocardial infarction syndrome or postcardiac injury syndrome.TNF, NOS3, ACE, TGFB1, HMGB1, IL1B, AGT, MMP2, MMP9, CASP3, NPPA, GSK3B, ICAM1, GATA4, CAT, PPARGC1A, S100B, BECN1, SOD2, PLN, PLAU, LTA, MIAT, BCL2L1, IL10, HSD11B2, MYH7, PSMA6, OLR1, PHACTR1, BRAP, MIA3, SH2B3, WDR12, ESR1, THBD, IL6, EPO, CXCL12, APOE, ITGB3, TNFSF4, PLAT, BCL2, F7, F5, LGALS2, F2, REN, P2RY12, NR3C2, TNNI3, KIF6, LGALS3, F13A1, ATM, LRP8, IL1RN, HP, TP53, KLK1, BAX, SOD1, NOS2, HSPA5, MIR145, JAK2, PAPPA, TIMP2, DDIT3, TM6SF2, GCLM, IL6R, GCLC, SELL, CKM, LAMP2, PRKCE, NRIP1, ACTA2, CRP, NPPB, MIR423, ATP1A1, SIRT1, CKB, MIR125B2, VWF, EDN1, DGKZ, CREB1, CREM, CCN2, VDAC1, BAK1, ACE2, IGF1, KLF13, ADRB2, PDE3A, AGTR1, LDHA, ADORA3, CCL2, MIR761, MFF, ANGPT1, IFNA2, GJA1, ADORA1, DAB2IP, GGT1, ADIPOQ, HMOX1, SERPINE1, MMP1, HIF1A, TNFRSF12A, MAPK1, NFE2L2, AKT1, SELP, THBS1, SIRT3, F3, CYBB, IL17A, SMAD2, FN1, POSTN, ADRB1, ANGPT2, AGER, CD36, C3, TNC, PDE5A, TNFRSF1A, CCL5, CYBA, CD59, REG1A, FLT1, ANXA5, CDKN1B, CSF2, CASR, EDNRA, CTSB, MTOR, MIF, COL3A1, NFKBIA, TBX5, TNFRSF1B, PGF, HSPD1, UTS2, PLAUR, ITGB1, TGFBR1, MYH6, TRPV1, MDH2, MDK, IGF1R, MEF2C, EDNRB, SFRP2, EGLN3, HAMP, KCNK2, MMP14, BNIP3, MMP13, SOCS1, SDC1, SMAD4, ADAMTS1, SPARC, OPA1, VCAN, BDKRB2, CAV3, BDKRB1, MAP1LC3A, EGLN1, APOH, TFPI, SLC27A1, VDAC2, CSNK2A1, DCN, CSNK2B, DAB2, EPOR, ATP5F1D, MFN2, EPAS1, AVPR1A, ITGA3, CACYBP, DVL1, DAG1, EDN2, AK1, CYP11B1, KCNJ2, RAD50, TXNRD1, PDGFD, APOB, RPS6KB1, LPA, SLPI, HADH, LPL, GSR, FIS1, TBX3, UTS2R, TEK, GJA5, TGFB2, GHRH, TGFBR2, TTN, LDLR, SHH, RANBP1, YBX1, G6PD, FZD2, LCAT, MEF2A, TLR4, PCSK9, MAP3K5, BIRC5, IL4R, SLC27A6, PTN, PLCB3, OPRK1, ATG7, CCR3, TNFRSF14, COL1A1, ABO, CFL1, PPARG, PLCB1, CCNA2, OPRD1, PEBP1, C7, C8A, C8B, AIMP1, ABCA1, BTN2A1, SMAD3, CDKN2B-AS1, COL4A2, CTNNB1, ENPP1, ILF3, CLEC16A, LAMA3, FOS, ELN, MEFV, LDLRAP1, FAS, GLA, CAV1, GUCY1A1, IL23R, CBS, AP3D1, LRPAP1, IL12B, LIPA, ATP2B1, IRF5, LRP6, RNF13, STAT4, CFTR, MAPKAP1, PLCL2, ATL1, ITIH3, SMARCA4, CALR, BCHE, LMNA, HLA-B, JCAD, CYP17A1, ABCG5, DNAJC6, SPTBN5, RAF1, PLA2G6, MB, GCG, SORCS2, CXCR4, EMC8, PON1, MARCHF10, BAZ1B, THOC2, PIK3CG, PIGQ, OSGIN1, ZC3H3, GJA4, DYRK1B, PIGA, LZTR1, IVD, GTF2IRD1, CETP, PTPN11, ZC3HC1, ACSS1, CYP2C19, SCNN1A, CAD, YTHDF3, NLRP3, CDKN2A, ITGA1, NDST1, PLPP3, PECAM1, TSPO, ITPK1, NUP210, PTPRN2, FUT7, ABCC6, C20orf181, CD14, GLP1R, JPH3, TSPAN9, GTF2I, ABCG8, STAT3, CEP19, LARGE2, SRP54, PIK3CB, PML, MORF4L1, BRAF, HGD, HGF, NRG1, PIK3CD, DNAJC21, PITRM1, CSF3, SBDS, CST2, APOA1, TFF1, PIK3CA, GNB3, RFC2, APOC3, MAPK14, SLC2A10, TET2, MLX, PLA2G3, KLRC4, RGS12, LTBP2, VOPP1, CUL9, GP6, TAF4, GDF15, COL13A1, PDZD2, LIMK1, ERGIC1, POM121L9P, FGF2, BHMG1, ATXN2, SELE, CLCN1, SLC7A8, AVP, CELSR2, MTHFR, PSMB4, ALOX5, ALOX5AP, UGGT2, ZNF536, WNK2, ABCC1, VEGFA, MPO, AGPAT2, NCOR2, MPL, MALAT1, ANKUB1, SBF1, C9orf139, MYH9, BSCL2, TBL2, IL12A-AS1, MCCC2, TENM3, TRDMT1, IL12A, MMRN1, DPP4, GPR160, WRN, EIF2AK1, PSMA4, CLIP2, SEC24D, ALDH2, CCR1, PGR-AS1, BIN1, BCRP1, UBAC2, ARVCF, PLA2G2A, CCR2, POU2F3, MIR21, PLA2G1B, GPR135, PTGS2, TP73, CAVIN1, CPLX2, TCF25, SEPTIN9, DIDO1, UHRF1, FES, PLA2G7, FGB, SLC5A2, F10, TRAPPC9, C4A, SERPINA5, MMP3, SCNN1G, ERAP1, CYP27A1, CHRM3, SCNN1B, CCT2, IL1A, IKZF1, PLG, ITGA2, POLDIP2, AIMP2, RNF19A, AHSA1, APOA5, CRK, GRAP2, ADD1, ACCS, DECR1, GABPA, MIR499A, ACSS2, CCR5, ABCB1, PLA2G15, FSD1L, FSD1, ACTB, AGTR2, IKZF5, TM7SF2, PTEN, ADM, TNNT2, CYP2J2, CYP2C9, MTCO2P12, FGF23, TIMP1, CHDH, COX2, CX3CR1, ALB, PARP1, TXN, CFH, CYP2C8, THBS4, KDR, MIR34A, MSC, BDNF, LTA4H, FSTL1, ADAMTS13, CXCL8, GH1, MIR208A, TRS-AGA2-3, ADRA2B, MTR, ESR2, PTGIS, MAPK3, PROC, AHSG, IL4, MIR143, HFE, TBPL1, MBL2, GSTM1, CASP1, ITGA2B, SLC33A1, HPSE, GP1BA, CD34, HSPB3, EHMT1, HSPB1, IL18, MIR155, PPARA, APLN, CDKN2B, LCN2, ANXA1, PTK2B, FABP3, SORT1, OR10A4, MAPK8, S100A4, PTH, TNFRSF11B, ADAM8, NOS1, NM, NGF, ADH1C, OSM, FTO, PTGS1, AKR1A1, CIITA, MDM2, NT5E, PTX3, RLN2, ROS1, LIPC, LEP, MMP12, GPT, ARNTL, F2R, APOA4, SPP1, ST2, NR3C1, NOX4, NR1I2, TH, RIPK3, THPO, TIMP3, TLR2, FGA, COPD, C1QTNF9, VCAM1, LRPPRC, CHI3L1, ENG, MIR210, EGFR, DSPP, MIR126, DNASE1, MIR144, MIR17, CST3, CLU, CNR2, CPB2, SMUG1, SOAT1, COL4A1, MIR325, IL6ST, NTN1, IFNG, VPS51, HSPB2, SLC6A4, SHBG, ID2, MST1, GPR162, KLF4, EGR1, KIT, E2F1, ALOX12, HAVCR1, ATG5, ALOX15, C4B, PTGER4, VDR, GDF11, CCL11, EPRS1, PRKAB1, PRKAA2, TNFRSF4, SLC7A9, PCYT1A, DDX39A, KCNMA1, DES, BMI1, XRCC1, TREM1, INSRR, MYDGF, TLR9, BGN, NPR3, ABCG1, SERPINB2, ILK, NPY, GAS5, TRIB1, CTSD, CYP1A2, NFKBIL1, DDX39B, NFKB1, MIR146A, CYP11B2, SCG2, ADAMTS7, SERPINA3, MME, F11, TTR, BRCA1, THBS2, LBP, FABP4, ZGLP1, DNM1L, MIR208B, YAP1, PROM1, TFAM, COL18A1, SERPINF1, ACKR3, PER2, CD151, GSTP1, GSTT1, SELENBP1, SOCS3, CD40, SEMA6A, RUNX1, XPR1, AQP9, ITGAM, MIR223, MIR22, FAP, PRKAA1, S100A9, S100A8, FGF1, MGP, PDE4D, TMSB4X, RETN, FGG, TIMP4, ARG1, ANPEP, FUS, FPR2, CXCR6, DDAH2, PROCR, CLOCK, APOM, CREG1, LPAR2, CD163, MRAS, PRKCB, PRKCA, TXNRD2, PPIA, PADI4, TNFSF10, LIPG, ACSL6, UTRN, DENR, UGT1A1, TCP1, DUOX2, BAG3, DELEC1, KCNQ1OT1, SSTR4, SREBF2, NR1H3, INSIG2, SOD3, SMN2, RYR2, TGFBR3, SMN1, SLC25A37, EBI3, S100A1, SLC2A1, ACSL5, SEMA3F, CCHCR1, ATXN1, SDC4, DUOX1, SEMA3A, SLC52A1, DDAH1, BEST1, BHLHE40, FCN3, APOL1, DAPK2, KLK4, HDAC4, KDM3A, MTHFD1L, NES, RAPGEF5, XPO1, MEG3, MOK, INTU, PDCD4, UCP2, ANGPTL3, KCNE2, SETD2, NEIL3, PTPN1, TLR3, RCBTB1, THY1, PTGES, LOX, FBN1, BRS3, IL33, COL4A3, GLI3, C5AR1, IL15, C5, CXCL10, INS, PDX1, MIR326, GIPR, GHSR, COMT, BSG, MIR375, IGF2, COX8A, KCNQ1, KNG1, BMP2, ZNF627, GAP43, LIF, CRMP1, MIR183, CCND1, FNDC5, FLNA, LTC4S, FOXM1, IGF2R, CNR1, ADM2, CCND2, GSTM2, MIR29B1, MIR29B2, GSN, MIR23A, MIR30A, MIR30B, CD68, CYP2R1, CD40LG, ENTPD1, SCARB1, CD28, LRG1, CXCL1, PRRT2, MIR98, HSPA4, CGAS, CMA1, CAST, PLB1, GPR42, TXNRD3, GPER1, MIR203A, ZFAS1, AZIN2, IFNA1, IFNA13, SMAD1, LIFR, SERPINC1, CYP4A11, BTBD8, ENPEP, CYP1B1, ELANE, ACHE, MTAP, MIR150, F13B, MIR711, F2RL1, BRINP3, ETV2, CYP19A1, AIRE, CXCL16, GOLGA6A, NCAM1, NPPC, ACVR1B, GRK2, NPR1, PCSK1, NANOS3, NUCB2, ADRA1A, EPHX1, MPI, HPSE2, FOXO4, CTSK, PKD1, MIR590, PIM1, MIR106B, MCAM, ARSA, MIR100, TAS2R50, FCN2, AR, FCN1, MIR132, CTSG, DNTT, PF4, KMT2A, APEX1, APOC1, MIRLET7I, PFN2, MIR134, MIR140, MIR204, MIR221, MIR224, MIR139, MIR212, MIR130A, ERAL1, MIR206, AATF, MIR24-1, SIRT4, ADGRL3, MIR214, LPAR3, VPS33B, MIR199A1, MIR181A2, SH2B1, SOSTDC1, MIR181C, MIR185, MIR26A1, TXN2, GCA, MIR186, MIR15A, MIR188, MIR192, MIR197, MIR199A2, CLEC4E, MIR154, MIR19A, MIR19B1, DGCR5, PHGDH, MIR149, MIR15B, MIR20A, POFUT1, MIR142, MIR200A, BRD4, ANGPTL2, ARC, PALLD, MIR26B, KIF28P, MIR4306, MIR762, TMED7-TICAM2, LYVE1, CPSF4, MIR1908, JTB, MIR1825, MIR1231, MIR298, LILRB1, KIF2C, HOTAIR, WWP2, HNRNPUL1, MIR577, KIF3A, MIR421, CXADRP1, POTEM, APELA, MICA, MIR519D, NFAT5, H3P10, DCTN6, H3P24, H3P23, B3GNT2, LOC110806262, NRG3, RN7SL263P, OGA, TCFL5, PPR1, CST12P, TRAF3IP2, CERNA3, ARPP21, TP53COR1, APOC4-APOC2, TUBGCP2, COMMD3-BMI1, KLRC4-KLRK1, MIR486-1, SLC2A6, MIR27A, MIR34C, GPR166P, FAIM2, DNAI1, KDM1A, VN1R17P, POTEKP, EIF2AK4, PHLPP2, MIR93, MIR31, MIR148B, TBC1D9, MIR30E, MPRIP, STAB1, ABRAXAS2, METAP1, MLC1, MIR301A, MIR29A, MIR133B, SCAP, WIF1, FCMTE2, AKAP10, PADI2, MIR525, MIR498, MIR497, CHP1, ACOT7, MIR494, MIR146B, MIR424, MIR151A, MGLL, MIR370, MIR367, MIR328, CARD8, KLRK1, CD93, ATF6, SIRT2, MIR125A, TENM2, MIR122, AGGF1, DDIT4, TCHP, KBTBD7, REG4, TSPAN10, HMCN1, ROPN1L, FERMT3, TRPM4, CELF1, CNNM2, SESN2, NCAPG2, CASZ1, MAP1LC3B, TET1, ELOVL2, SARS2, ZC3H12A, TUG1, AGBL2, COQ5, CCDC93, AKT1S1, TSLP, HDAC7, GDE1, IL17F, GHRL, CLEC6A, MYOCD, DERL3, ZNF160, WNT3A, ABCC11, HHIPL1, TERF2IP, XRN1, ATAD1, ADTRP, PSRC1, RNASE7, IL1F10, DOT1L, PCDH18, KLF3-AS1, RMDN3, MIR10A, RHBDF2, EAF2, GREM2, STRA6, TINAGL1, MOAP1, ELOVL5, LGR6, BTNL2, ZNF77, CREBZF, SLC2A9, CELF4, STARD7, NGB, PTBP2, TRIB3, TBX20, MRTFA, JPH2, PELI1, CFAP97, ST6GALNAC1, TTTY15, GINGF2, PPP6R3, NDNF, ADIPOR2, OGFOD1, SLC52A2, CDC73, PAGR1, NOX5, ELOVL6, TRPM8, NBEAL1, NUCKS1, ACD, FEM1A, CDCA7L, MRPS6, CDCP1, AIDA, SMPD4, SYBU, SLC30A6, RAB14, TMEM54, SIRT6, ISYNA1, TMOD4, NCR3, COL6A5, IL27, SPESP1, GPRC6A, ZBTB12, DIPK2A, LINC00528, MLKL, DCP1B, RHOV, THAP5, OXER1, NENF, HFM1, CITED4, CCDC63, TMTC3, SPAAR, ZNF746, MRGPRX1, ASPM, NEAT1, OSTN, HSPB7, MIRLET7D, PEAR1, IL37, DISC1, GSTK1, TICAM2, SLC6A18, ACTBL2, HPGDS, EMC10, TNRC6A, CPP, STING1, RABGEF1, PPP1R42, SGSM3, MAT2B, REM1, ATP10D, IL19, PPM1L, A1CF, CPA4, GPR151, SLCO6A1, ANGPTL4, HSPB6, EARS2, JDP2, MRGPRX4, PLEKHO1, HSPA14, MRGPRX3, MUC17, HSPA12B, LRRC3B, BFAR, OMA1, TLR7, FBXO32, PLA1A, C1QTNF5, TRPV2, RMDN1, ADIPOR1, KCNIP2, ASCC1, RMDN2, ERFE, COMMD7, GNAS-AS1, MOB3C, IL22, NTM, MMVP1, TMED5, TMED7, TNNI3K, GLRX2, PTPRVP, B3GNTL1, IL34, PWAR1, APIP, GAL, CACUL1, TRPM6, A2M, CX3CL1, TXNIP, GCH1, GLO1, GFAP, GDF10, MSTN, GDF1, GCKR, GCGR, FXN, GC, GATA3, GAS6, GARS1, FYN, FUT4, GLRA2, GOLGA4, GPI, GPLD1, CXCR3, GPR17, GRK4, GPX1, GPX4, GRB2, GRIA1, CXCL2, GUCY1B1, GYS1, GZMB, HABP2, SERPIND1, GAST, FPR1, SLCO1B1, EPHB4, F9, EZH2, ESRRA, ERBB4, ERBB2, EPHX2, EPHB2, FOLR2, ENO2, ENO1, MARK2, EIF4EBP1, EFNA3, S1PR3, FABP2, FANCD2, FAT1, FBP1, FCAR, FCGR2A, FCGR3A, FCGR3B, FER, FGF9, FGFR1, FGFR3, FOXO1, FOXO3, FLT4, FOLH1, FOLR1, HDAC1, HHEX, HIC1, KLKB1, LCP1, RPSA, LAIR1, LAD1, KRT16, KRT1, KCNN4, HLA-C, KCNJ11, KCNE1, ITIH4, ITGB2, ISL1, IRF6, LCT, LEPR, LGALS3BP, LIPE, LRP1, LTB, CYP4F3, CD180, LYN, TACSTD2, SMAD7, MAG, MAP4, MAPT, MAS1, MBNL1, MCL1, IRF3, ITGA6, IPP, HTR1D, HLA-DMB, HLA-DPB2, HMGB2, HMGCR, HMGA1, NR4A1, HRG, HSD11B1, HSF1, HSPA1A, HSPA1B, HSPA1L, HSPA9, HSP90AA1, HTR2A, INHBA, ICAM3, IRF8, IFI27, IFNAR1, IFNGR2, IGFBP1, IGFBP3, IGFBP4, IGFBP7, IL2RB, CXCR1, CXCR2, IL11, TNFRSF9, S1PR1, ECM1, ECE1, BACH1, BMP6, CXCR5, BID, CEACAM1, CFB, BCL2A1, BAAT, RUNX3, B2M, AZU1, ATR, ATP5PF, ATOH1, ATF3, BNIP3L, BPI, BRCA2, KLF9, BTK, SERPING1, C3AR1, C9, CA2, CA3, SLC25A20, CALCR, CALM2, CAMP, CANX, CASP7, CASP8, ASPA, ASIP, ARR3, APLNR, ABCA4, AOC1, ACACA, ACACB, ACTG1, ACTG2, ADA, ADAM10, ADH1B, ADH5, ADORA2B, ADRB3, AGRP, JAG1, AHR, AREG, AKT2, ALCAM, AMPD1, ANG, ANK2, ANXA7, APAF1, APC, APOA2, APOC2, APOC4, APOD, APP, APRT, CASP9, CCK, E2F4, CTSZ, DBH, CYP7A1, CYP3A4, CYP2D6, CYP1A1, CXADR, CTSE, CD5L, NKX2-5, CSH2, CSH1, CRY2, CRX, CR1, DBP, DCC, DDT, DHCR24, SEPTIN1, DIO3, DLD, DMD, DNMT1, DNMT3A, DRD1, ATN1, RCAN1, TSC22D3, HBEGF, DUSP1, DYRK1A, CPT2, CPT1A, CPOX, CENPC, CD27, CD44, CD69, CDK1, CDC42, CDH2, CDH11, CDH13, CDKN1A, CDKN1C, CDX2, CEACAM5, CEBPD, CECR, CEACAM3, CPA3, CEACAM7, CHAT, CHGA, CHRNA4, CHRNA5, CHUK, CKMT2, ERCC8, CCR7, CNP, COL1A2, COL5A2, COMP, CP, CD46, MEIS2, MAP3K3, SF3A2, GPR65, LOH19CR1, FZD7, FZD4, FZD1, MIA, ECB2, FGF16, GHS, ALMS1, PXDN, DNALI1, ZNF202, YWHAZ, RAE1, RGS5, PPM1D, CYP4F2, MAPKAPK5, DEGS1, TNFSF11, PDE8B, RTCA, AOC3, SLC4A4, VAMP8, RIPK1, TNFSF13, DLK1, TNFRSF11A, IL18R1, XRCC3, XIST, XBP1, TPD52, TAC1, ADAM17, TBXA2R, TBXAS1, ZEB1, TRA, PPP1R11, TERT, TGFB3, TGM2, CLDN5, TNFAIP6, TNNI2, TNXB, TRPC3, WT1, TRPC4, TTC3, TTPA, TYR, SUMO1, UCP3, VEGFB, VEGFC, VIM, VIP, VLDLR, WARS1, WNT1, WNT11, FGF18, NRP1, ABCC8, HDAC6, NAMPT, BCAP31, PPIF, ABCC9, ABCB6, GJC1, NR2E3, TMEM11, DGCR2, NR1H4, NR1I3, MVP, GFPT2, TOMM70, ATP6AP2, MPZL2, TRIM13, STX6, RAMP1, CNPY2, WARS2, PRMT5, GPNMB, MERTK, FST, CARM1, ZNRD2, UBD, ANP32B, SLC35A1, GNLY, KEAP1, BMS1, SNX17, KL, CFLAR, CCN4, PER3, IER3, ARHGEF7, FUBP1, WASF1, TRPA1, ARTN, DNAJA3, LRRFIP1, AURKB, IL32, PPIG, COX5A, PIEZO1, RECQL5, FADS2, MED23, QKI, GSTO1, FHL5, GAL3ST1, SPTLC2, GOSR1, GOSR2, AKAP12, PRORP, PPP6R2, EIF4A3, SUV39H1, STXBP2, MET, PIK3C2G, PMM2, SERPINF2, PLD1, PLCB2, PLA2G4A, PITX3, SERPINA4, PROX1, PI3, PFN1, SLC26A4, PDK4, PDHB, PDGFRA, PNMT, POLD1, PON2, PPARD, PPID, PPP1R1A, PRF1, PRH1, PRH2, PRKAR1A, PKN1, PRKD1, MAPK10, MAP2K1, MAP2K6, PRL, PRNP, PDGFA, PDCD1, PCSK2, MYD88, MFAP1, KITLG, CXCL9, MITF, MMP7, MMP8, MRE11, MSRA, MT1JP, COX1, MTHFD1, ND2, MTTP, MYBL2, MYLK, PCNA, NAB1, NDUFA2, NTRK2, OGG1, OGN, SLC22A18, P2RX7, P2RY1, P2RY2, P4HB, PAK1, PAM, PRKN, PC, PROS1, MASP1, STXBP1, SLC5A5, SLN, SLC25A1, SLC16A1, SLC6A8, SLC6A6, SLC6A3, SLC5A3, PSEN1, SMTN, SLC5A1, SLC2A4, ST3GAL4, SIAH2, SGK1, SMARCA1, SMPD1, SMPD2, SNAI1, SNRNP70, SOX9, SP1, SP3, SPG7, SPRR2A, AKR1D1, SRY, SSTR2, STAT6, SULT1E1, ELOVL4, STIM1, SRSF3, SELENOP, SELPLG, RFC1, PSG2, PSMD9, PSMD10, PTBP1, PTGDS, PTGER2, PTK2, PTPRA, PTPRC, PZP, RAC1, RAP1A, RASGRF2, RENBP, RNASE1, CXCL6, RNASE2, RPGR, RPS19, RPS20, RRAD, RYR3, S100A12, SAA1, SAFB, SCN5A, CCL19, CCL20, CCL21, CCL22, H3P40
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Rh Disease
Wikipedia
CS1 maint: multiple names: authors list ( link ) External links [ edit ] National institute of Clinical Excellence (NICE) Guidelines for anti-D prophylaxis Summary of transfusion reactions in the US Classification D ICD - 10 : P55.0 ICD - 9-CM : 773.0 MeSH : D012203 External resources MedlinePlus : 001600 v t e Conditions originating in the perinatal period / fetal disease Maternal factors complicating pregnancy, labour or delivery placenta Placenta praevia Placental insufficiency Twin-to-twin transfusion syndrome chorion / amnion Chorioamnionitis umbilical cord Umbilical cord prolapse Nuchal cord Single umbilical artery presentation Breech birth Asynclitism Shoulder presentation Growth Small for gestational age / Large for gestational age Preterm birth / Postterm pregnancy Intrauterine growth restriction Birth trauma scalp Cephalohematoma Chignon Caput succedaneum Subgaleal hemorrhage Brachial plexus injury Erb's palsy Klumpke paralysis Affected systems Respiratory Intrauterine hypoxia Infant respiratory distress syndrome Transient tachypnea of the newborn Meconium aspiration syndrome Pleural disease Pneumothorax Pneumomediastinum Wilson–Mikity syndrome Bronchopulmonary dysplasia Cardiovascular Pneumopericardium Persistent fetal circulation Bleeding and hematologic disease Vitamin K deficiency bleeding HDN ABO Anti-Kell Rh c Rh D Rh E Hydrops fetalis Hyperbilirubinemia Kernicterus Neonatal jaundice Velamentous cord insertion Intraventricular hemorrhage Germinal matrix hemorrhage Anemia of prematurity Gastrointestinal Ileus Necrotizing enterocolitis Meconium peritonitis Integument and thermoregulation Erythema toxicum Sclerema neonatorum Nervous system Perinatal asphyxia Periventricular leukomalacia Musculoskeletal Gray baby syndrome muscle tone Congenital hypertonia Congenital hypotonia Infections Vertically transmitted infection Neonatal infection rubella herpes simplex mycoplasma hominis ureaplasma urealyticum Omphalitis Neonatal sepsis Group B streptococcal infection Neonatal conjunctivitis Other Miscarriage Perinatal mortality Stillbirth Infant mortality Neonatal withdrawal
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Kyasanur Forest Disease
Wikipedia
External links [ edit ] Classification D ICD - 10 : A98.2 ICD - 9-CM : 065.2 MeSH : D007733 External resources Orphanet : 319254 v t e Zoonotic viral diseases (A80–B34, 042–079 ) Arthropod -borne Mosquito -borne Bunyavirales Arbovirus encephalitides : La Crosse encephalitis LACV Batai virus BATV Bwamba Fever BWAV California encephalitis CEV Jamestown Canyon encephalitis Tete virus Tahyna virus TAHV Viral hemorrhagic fevers : Rift Valley fever RVFV Bunyamwera fever BUNV Ngari virus NRIV Flaviviridae Arbovirus encephalitides : Japanese encephalitis JEV Australian encephalitis MVEV KUNV Saint Louis encephalitis SLEV Usutu virus West Nile fever WNV Viral hemorrhagic fevers : Dengue fever DENV-1-4 Yellow fever YFV Zika fever Zika virus Togaviridae Arbovirus encephalitides : Eastern equine encephalomyelitis EEEV Western equine encephalomyelitis WEEV Venezuelan equine encephalomyelitis VEEV Chikungunya CHIKV O'nyong'nyong fever ONNV Pogosta disease Sindbis virus Ross River fever RRV Semliki Forest virus Reoviridae Banna virus encephalitis Tick -borne Bunyavirales Viral hemorrhagic fevers : Bhanja virus Crimean–Congo hemorrhagic fever (CCHFV) Heartland virus Severe fever with thrombocytopenia syndrome ( Huaiyangshan banyangvirus ) Tete virus Flaviviridae Arbovirus encephalitides : Tick-borne encephalitis TBEV Powassan encephalitis POWV Viral hemorrhagic fevers : Omsk hemorrhagic fever OHFV Kyasanur Forest disease KFDV AHFV Langat virus LGTV Orthomyxoviridae Bourbon virus Reoviridae Colorado tick fever CTFV Kemerovo tickborne viral fever Sandfly -borne Bunyavirales Adria virus (ADRV) Oropouche fever Oropouche virus Pappataci fever Toscana virus Sandfly fever Naples virus Rhabdoviridae Chandipura virus Mammal -borne Rodent -borne Arenaviridae Viral hemorrhagic fevers : Lassa fever LASV Venezuelan hemorrhagic fever GTOV Argentine hemorrhagic fever JUNV Brazilian hemorrhagic fever SABV Bolivian hemorrhagic fever MACV LUJV CHPV Bunyavirales Hemorrhagic fever with renal syndrome DOBV HTNV PUUV SEOV AMRV THAIV Hantavirus pulmonary syndrome ANDV SNV Herpesviridae Murid gammaherpesvirus 4 Bat -borne Filoviridae BDBV SUDV TAFV Marburg virus disease MARV RAVV Rhabdoviridae Rabies ABLV MOKV DUVV LBV CHPV Paramyxoviridae Henipavirus encephalitis HeV NiV Coronaviridae SARS-related coronavirus SARS-CoV MERS-CoV SARS-CoV-2 Primate -borne Herpesviridae Macacine alphaherpesvirus 1 Retroviridae Simian foamy virus HTLV-1 HTLV-2 Poxviridae Tanapox Yaba monkey tumor virus Multiple vectors Rhabdoviridae Rabies RABV Mokola virus Poxviridae Monkeypox v t e Tick-borne diseases and infestations Diseases Bacterial infections Rickettsiales Anaplasmosis Boutonneuse fever Ehrlichiosis ( Human granulocytic , Human monocytotropic , Human E. ewingii infection ) Scrub typhus Spotted fever rickettsiosis Pacific Coast tick fever American tick bite fever rickettsialpox Rocky Mountain spotted fever ) Spirochaete Baggio–Yoshinari syndrome Lyme disease Relapsing fever borreliosis Thiotrichales Tularemia Viral infections Bhanja virus Bourbon virus Colorado tick fever Crimean–Congo hemorrhagic fever Heartland bandavirus Kemerovo tickborne viral fever Kyasanur Forest disease Omsk hemorrhagic fever Powassan encephalitis Severe fever with thrombocytopenia syndrome Tete orthobunyavirus Tick-borne encephalitis Protozoan infections Babesiosis Other diseases Tick paralysis Alpha-gal allergy Southern tick-associated rash illness Infestations Tick infestation Species and bites Amblyomma Amblyomma americanum Amblyomma cajennense Amblyomma triguttatum Dermacentor Dermacentor andersoni Dermacentor variabilis Ixodes Ixodes cornuatus Ixodes holocyclus Ixodes pacificus Ixodes ricinus Ixodes scapularis Ornithodoros Ornithodoros gurneyi Ornithodoros hermsi Ornithodoros moubata Other Rhipicephalus sanguineus Taxon identifiers Wikidata : Q19838389 IRMNG : 11460133 NCBI : 33743
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Liver Disease
Wikipedia
Liver disease Other names Hepatic disease Micrograph of non-alcoholic fatty liver disease Specialty Gastroenterology Types Fatty liver disease , Hepatitis (and several more) [1] Diagnostic method Liver function tests [2] Treatment Depends on type(See types) Liver disease (also called hepatic disease ) is a type of damage to or disease of the liver . [1] Whenever the course of the problem lasts long, chronic liver disease ensues. [ citation needed ] Contents 1 Signs and symptoms 2 Cause 3 Mechanism 3.1 DNA damage 3.2 Other relevant aspects 3.3 Air pollutants 4 Diagnosis 5 Treatment 6 See also 7 References 8 Further reading 9 External links Signs and symptoms [ edit ] Some of the signs and symptoms of liver disease are the following: Jaundice [ citation needed ] Confusion and altered consciousness caused by hepatic encephalopathy . [ citation needed ] Thrombocytopenia and coagulopathy . [3] Risk of bleeding symptoms particularly taking place in gastrointestinal tract [4] Cause [ edit ] Ground glass hepatocytes Primary biliary cirrhosis Budd-chiari syndrome There are more than a hundred different kinds of liver disease. ... Analogous terms such as "drug-induced" or "toxic" liver disease are also used to refer to disorders caused by various drugs. [8] Fatty liver disease (hepatic steatosis ) is a reversible condition where large vacuoles of triglyceride fat accumulate in liver cells. [9] Non-alcoholic fatty liver disease is a spectrum of disease associated with obesity and metabolic syndrome . [10] Hereditary diseases that cause damage to the liver include hemochromatosis , [11] involving accumulation of iron in the body, and Wilson's disease . ... Liver transplantation can give a curative treatment option. [14] Gilbert's syndrome , a genetic disorder of bilirubin metabolism found in a small percent of the population, can cause mild jaundice . [15] Cirrhosis is the formation of fibrous tissue ( fibrosis ) in the place of liver cells that have died due to a variety of causes, including viral hepatitis, alcohol overconsumption, and other forms of liver toxicity. ... (Many liver malignancies are secondary lesions that have metastasized from primary cancers in the gastrointestinal tract and other organs, such as the kidneys, lungs.) [17] Primary biliary cirrhosis is a serious autoimmune disease of the bile capillaries . [18] Primary sclerosing cholangitis is a serious chronic inflammatory disease of the bile duct , which is believed to be autoimmune in origin. [19] Budd–Chiari syndrome is the clinical picture caused by occlusion of the hepatic vein . [20] Mechanism [ edit ] Liver disease can occur through several mechanisms: DNA damage [ edit ] One general mechanism, increased DNA damage, is shared by some of the major causes of liver disease. ... Retrieved 2015-06-20 . ^ "Gilbert syndrome" . Genetics Home Reference . Retrieved 2015-06-20 . ^ "Cirrhosis: MedlinePlus Medical Encyclopedia" . www.nlm.nih.gov .ABCB4, SERPINA1, AFP, GPT, TNF, GGT1, NR1H4, ATP7B, NPC1, CCL2, MMP9, HMOX1, NOS2, NFKB1, CCR2, MTHFR, SCO1, CSF3, HSPA1A, SORT1, SRSF5, TIMP3, NQO1, CRISPLD2, ALPL, HPGDS, COL3A1, CYP7B1, SC5D, IL1RAP, LTB4R, ENO3, MRPS23, TYROBP, CD86, TXN, CD3D, RNASE6, CCK, SOD1, IL1R2, DDAH1, TM4SF4, ACTA2, SOCS1, IL11, HK3, TREM1, IL9R, BCL2L1, INS, GNG8, GABRR2, CD79B, AHR, JUP, ALAD, CYP2E1, GRK5, NRP1, RAC1, TGM1, ALOX5AP, SOCS3, AMACR, ASAH2, ITGB6, SULT1E1, SERPINE1, CCR1, ST8SIA1, CYP1A2, LAT, FAS, TRMU, DPYD, MDM2, HLA-DOA, DNAJA2, FASLG, ARG1, TM6SF2, IFNA1, GOLM1, ALB, IL10, MIR122, PNPLA3, KRT18, SPP1, NFE2L2, HLA-DRB1, IL18, HAMP, FBL, ABCB11, IL6, IFNL3, HFE, IFNA13, TGFB1, SLC17A5, IL17A, UGT1A1, TP53, IFNG, HGF, TLR4, ADIPOQ, GGTLC4P, ATP8B1, GGTLC5P, GGT2, GGTLC3, FECH, GABPA, APOE, IL33, CXCL10, IL1B, PPIG, F2, KRT8, ALDH2, LOC102724197, GGTLC1, LEP, REN, RBM45, LGALS3BP, CCL4, CYP2B6, GCG, STAT4, FAH, IL22, PPARA, CFTR, ADH1C, CD14, MBL2, CDKN2A, ABCD1, XPR1, NLRP3, TIMP1, GPBAR1, HAVCR2, ADH1B, CXCL12, GOLPH3, CYP2C19, CHI3L1, TLR3, IGF1, CCR5, BCL2, TERT, CTNNB1, PTEN, CCN2, FGF21, VIPR1, ABCC2, IL2, IGFBP1, IL1RN, IL4, APLN, TNFRSF1B, CXCL8, TLR2, CP, IGF2, SIRT1, CD1D, CD40, EXT1, IL1A, MMRN1, IL37, IFNA2, GFER, AKT1, LIPA, ACTB, AKR1B10, IL21, PTGS2, GSTP1, PRKCSH, VDR, MTTP, GNMT, NAT10, GDF2, HLA-DQA1, ATHS, H3P10, VWF, VTN, MBOAT7, ANGPT1, SLPI, PDCD1, AKR1A1, MIR34A, HADHA, CCL27, ADAMTS13, ACE2, CX3CL1, PIK3CA, ALPP, PIK3CG, NOS3, PIK3CD, ASRGL1, PIK3CB, PF4, TNFRSF11B, VEGFA, LTA, MIR223, CYP3A4, THPO, CEACAM5, DGUOK, SERPINA3, FGF19, ACE, CYP7A1, PDLIM3, STAT3, CYP2D6, SMAD3, MAPK1, CST3, LGALS3, MAPK14, CR1, NR1I2, DDC, ESR1, PON1, SST, TMBIM4, ATRNL1, IL23A, PPARG, LBP, PTPN1, LCN2, POLDIP2, FST, RETN, POSTN, CD274, MPI, RDX, HLA-DPB1, RNF19A, PSG2, SLCO1B1, HLA-DRB3, LMNA, ABCB6, KRAS, PAEP, HNF4A, KDR, MGMT, LARS1, PRKAB1, TNFRSF12A, CXCL9, ATP6AP2, RIPK3, SLC25A13, COX2, RBP4, UGT1A7, PGF, HP, GDF15, PTPN2, MMP2, PKHD1, DEPDC5, SLC5A2, AHSA1, CCL5, REXO1L1P, CTLA4, RIPK1, HNF1B, STS, TAP2, CYP1A1, TAP1, CYP2A6, CYP2C9, TNFSF10, IL23R, TXNRD1, TAC1, DECR1, DLAT, APOC3, TFEB, DNASE1, DPP4, APOA1, MICOS13, UBE2B, EGF, MIR200A, ENG, HIF1A, PCSK9, UCP2, CRP, MIR192, TM7SF2, CASP1, TNFAIP6, CASP3, CD19, MIR146A, OPN1SW, BCHE, CDKN1A, MIR221, ATP6AP1, CEBPA, THBS1, CEACAM3, CEACAM7, CLU, TNFSF11, CCR6, HSD17B6, AIMP2, TERC, SERPINC1, BTBD8, CRK, SRY, ST2, MICA, GNAS, ERN1, MSC, ADH1A, GHR, SHBG, GPC3, PSC, IFNL4, CD163, GLI2, GLO1, MTCO2P12, GAPDH, SDC1, CXCL2, LOC110806263, ERVK-6, GSTM1, CXCL16, CXCL11, GRAP2, CCL21, CCL20, ABCG2, DCLK1, BPI, YY1, ANXA2, ANXA1, SOD2, FABP4, AGRP, LCS1, SMPD1, FLT1, F10, CXCR4, ARTN, WNT3A, ALDH1B1, COL18A1, ALDH1A1, AGT, F3, APEX1, FAT1, KMT2D, ST8SIA4, ABCC4, SLC7A5, ARHGEF5, PEMT, CPQ, C1orf61, TRIM22, TFPI2, XRCC1, PAK4, MERTK, CNBP, TFG, XRCC4, WARS2, ABCC3, SLC25A15, TAM, MGAM, SELENBP1, RAPGEF5, TM4SF5, PPP6R2, MRPL28, ISG15, AIP, RGN, PRDX6, HGS, APOBEC3B, IL32, H6PD, S1PR2, CCL4L2, CXCL14, CIR1, TBPL1, SLC9A3R1, FHL5, WASF1, TIMELESS, SQSTM1, IL18BP, KDM5D, WASF2, NR0B2, SOAT2, IKBKG, LGR5, NAMPT, KHSRP, LRPPRC, NR1H3, ARHGEF7, AOC3, BECN1, TNFSF13, NR1I3, TNFRSF10B, SLC23A1, GGH, SLC23A2, MFN2, NAT2, UGT1A6, IVNS1ABP, NLRP6, BHLHE23, CMPK2, REG3G, SLCO6A1, KLF14, TMEM199, IFNLR1, DDX53, BMPER, IMMP1L, EHMT1, MLKL, SPDYA, COPD, IFNL1, MIR7-3HG, STPG4, ATP11C, CELIAC2, HSD17B13, CLNK, CTHRC1, C1QTNF1, CYGB, CPEB4, PDCD1LG2, HM13, TRAPPC9, NBPF3, CCDC115, IL1F10, GPT2, PPP1R15B, KRT90P, TRIM5, GFM1, TSLP, DPP9, TMEM67, DNER, MUC16, SFXN1, IL17F, ACTBL2, ARSH, GSTK1, MIR25, MIR29A, MIR93, POTEKP, MIR338, MIR451A, DELYQ11, POTEM, MSMP, KRT8P3, ZGLP1, SYCE1L, MIR1224, LINC01672, KLRC4-KLRK1, MIR4717, ERVK-20, TP53COR1, ERVK-32, H3P9, MIR27A, MIR224, LRRC37A3, MIR22, ZNF699, SERPINA13P, CCL4L1, MIRLET7C, MIRLET7G, MIR101-2, MIR125A, MIR126, MIR136, MIR148A, MIR149, MIR155, MIR17, MIR18A, MIR191, MIR20A, MIR21, MIR212, MIR219A1, HSD3B7, LIN28A, IGF2BP1, SLC40A1, VPS33B, HAVCR1, NPHP3, SIGLEC7, GLS2, IL17B, ANGPTL3, SLCO1B3, NXT1, ERVW-1, MANEA, CD209, IL20, IL21R, NTM, ASCC1, SEPSECS, SBDS, DCTN4, ZDHHC2, KRT23, CHMP2B, BRD1, NUP62, KHDRBS1, CXCR6, TNFSF13B, FGL2, SUB1, CIT, PSIP1, RASSF1, SEC63, MAN1B1, ACOT7, NID2, KLRK1, PEG10, STAB1, GANAB, RPGRIP1L, POFUT1, SMUG1, CLEC1B, TLR7, CYP39A1, SPHK2, AICDA, BIRC6, CC2D2A, KLHL1, IGDCC4, ZNF410, RBPJP4, CIDEC, NOD2, XYLT2, CARD9, HIF3A, DCLRE1C, CPEB1, CDCP1, MPPE1, AHNAK, ADIPOR2, NEIL1, UGGT1, CFC1, ISYNA1, WDR11, SIRT6, NBAS, DNAJB11, CMPK1, TLR9, ANLN, CCHCR1, UGT1A10, UGT1A8, WT1, UGT1A5, UGT1A9, UGT1A4, UGT1A3, MARCHF5, DPP8, CHDH, IMPACT, RNPC3, XBP1, PTPRO, WNT2B, FUT1, FOXC1, FOXM1, FOXO3, FLNA, FMR1, FN1, MTOR, NR5A2, FUSE, FUT2, IL6ST, G6PC, GALT, GBE1, GC, GCK, GCKR, MSTN, GEM, GH1, FGFR3, FGF7, FGF2, FANCA, DSC3, DSPP, DUSP5, EDN1, EGFR, EGR1, EHHADH, ELN, EPAS1, EPHB2, EPHX1, ERBB4, ESR2, ETV3, EZH2, F5, F8, F9, FABP3, GIP, GJB2, GCLM, HMGB3, FOXA2, FOXA3, ONECUT1, HOXD13, HRC, HSD11B1, HSPA1B, HSPA4, HSPB1, HSPG2, HTR2A, ICAM1, IFNAR2, IGF2R, IGFBP2, IGFBP3, IGFBP6, CCN1, IKBKB, HMGCS2, HMGB1, GLP1R, HMBS, CXCR3, GRB2, GRN, CXCL1, GSPT1, GSTA1, GTF2H1, GUSB, HADH, HARS1, HAS1, HAS3, SERPIND1, HCLS1, HDAC1, CFH, HGFAC, HLA-A, HLA-DRB4, ATN1, SLC26A3, DOK1, ANPEP, XIAP, BIRC5, APLP2, APOB, AQP6, ABCC6, AREG, ASS1, ATD, RERE, ATP12A, ATP4A, AVP, BAGE, BCS1L, CEACAM1, BMP2, BMP4, BMP8B, AIRE, ANGPT2, BUB1, AMBP, ACACA, ACADM, ACADVL, ACHE, ACTG1, ACTG2, ACVRL1, ADAM8, ADAM10, ADAR, ADCYAP1, PLIN2, ADH5, AFM, AGER, JAG1, AGTR1, ALAS2, AKR1B1, BRCA2, SERPING1, DMRT1, COMT, CLDN3, CPOX, CREB1, CREBBP, CRYGD, CSF2, CSF3R, SLC25A10, CTSL, CTSS, CTSZ, CUX1, CYP1B1, CYP17A1, CYP51A1, DCX, AKR1C1, DDX3X, DMBT1, COX8A, COL1A2, VPS51, CNR2, CALR, CASP2, RUNX3, CD34, CD36, CD40LG, CD68, CD151, CDA, CDC25A, CDK4, CDKN2B, CDO1, CDSN, CES1, CFL1, CHUK, CLTC, CNR1, IL2RB, IL7R, WARS1, CCL22, ROS1, S100A4, S100A9, S100B, SERPINB3, SERPINB4, SCN2A, CCL17, CCL19, SELE, IL10RB, SELP, SELENOP, SRSF4, SI, ST6GAL1, ST3GAL4, SKIV2L, SLC2A1, SLC3A2, RORA, ABCE1, RNASE1, RIT2, SEPTIN4, POLG, PPARD, PRF1, PRKAA1, PRKAA2, PRKACA, PRKCZ, MAPK3, MAPK8, MASP1, RELN, PTPN6, PTPN11, PVR, RAD51, RARRES2, RENBP, REST, SLC4A1, SLC4A2, SLC10A1, TGFBR1, TIMP2, TKT, TLE1, TLL1, TLR5, TMSB4X, TNFAIP3, TNFRSF1A, TPMT, TPO, TRPC5, TYRP1, SLC35A2, UGT1A, UGT2B7, UMOD, UROD, VCAM1, VIP, THAS, TGFB2, SOX9, TEP1, SPINK1, SPINT1, SPRR2A, SPTBN1, SRD5A2, AKR1D1, SREBF2, STAT5A, STAT5B, SULT2A1, SYK, ADAM17, TALDO1, TBX1, TCF3, TCF7L2, ZEB1, TEAD1, TMBIM6, PMM2, PLA2G5, PKM, LIG4, CYP4F3, LTBP3, BCAM, SH2D1A, LYZ, EPCAM, SMAD7, MAGEA3, MAT2A, MDM4, MAP3K5, MET, MFGE8, MIA2, ATXN3, MLH1, NR3C2, MMP1, MMP3, LTB, LGALS9, MMP10, LEPR, IL13, IL15, IMPA1, IDO1, INSR, ITGA6, IRF6, IRF7, ISG20, ITPA, ITPR3, JAK2, JUN, KCNJ5, KIR3DL1, KNG1, KIF22, LCAT, LDLR, MMP7, MMP13, PKD1, NTS, OAS1, OAS2, OGG1, OLR1, OPRM1, OSM, OTC, PAH, PAK2, PAK3, PDGFRA, PDGFRB, ENPP2, SERPINF1, PEX1, ABCB1, PHB, PHKG2, PIM1, NUP88, YBX1, MOS, SLC11A2, MPL, ABCC1, MSH3, MT1B, MTAP, MUC2, MUC4, MVK, MYC, MYD88, MYO5B, NAGA, NCAM1, NGF, NGFR, NHS, NM, NOS1, CCN3, H3P40
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Vaginitis
Wikipedia
These symptoms are usually due to decreased hormones usually occurring during and after menopause . Current term is Genitourinary syndrome of menopause. alkaline Bacterial vaginitis ( B96.3 ). ... The former terms do not describe the negative effects on the lower urinary tract which can be the most troubling symptoms of menopause for women. ^ Portman, D.J.; Gass, M.L.S. (2014). "Genitourinary syndrome of menopause: New terminology for vulvovaginal atrophy from the International Society for the Study of Women's Sexual Health and The North American Menopause Society". ... External links [ edit ] Classification D ICD - 10 : N76.0 - N76.1 ICD - 9-CM : 616.1 MeSH : D014627 DiseasesDB : 14017 External resources MedlinePlus : 000897 eMedicine : med/3369 med/2358 emerg/631 emerg/639 v t e Female diseases of the pelvis and genitals Internal Adnexa Ovary Endometriosis of ovary Female infertility Anovulation Poor ovarian reserve Mittelschmerz Oophoritis Ovarian apoplexy Ovarian cyst Corpus luteum cyst Follicular cyst of ovary Theca lutein cyst Ovarian hyperstimulation syndrome Ovarian torsion Fallopian tube Female infertility Fallopian tube obstruction Hematosalpinx Hydrosalpinx Salpingitis Uterus Endometrium Asherman's syndrome Dysfunctional uterine bleeding Endometrial hyperplasia Endometrial polyp Endometriosis Endometritis Menstruation Flow Amenorrhoea Hypomenorrhea Oligomenorrhea Pain Dysmenorrhea PMS Timing Menometrorrhagia Menorrhagia Metrorrhagia Female infertility Recurrent miscarriage Myometrium Adenomyosis Parametrium Parametritis Cervix Cervical dysplasia Cervical incompetence Cervical polyp Cervicitis Female infertility Cervical stenosis Nabothian cyst General Hematometra / Pyometra Retroverted uterus Vagina Hematocolpos / Hydrocolpos Leukorrhea / Vaginal discharge Vaginitis Atrophic vaginitis Bacterial vaginosis Candidal vulvovaginitis Hydrocolpos Sexual dysfunction Dyspareunia Hypoactive sexual desire disorder Sexual arousal disorder Vaginismus Urogenital fistulas Ureterovaginal Vesicovaginal Obstetric fistula Rectovaginal fistula Prolapse Cystocele Enterocele Rectocele Sigmoidocele Urethrocele Vaginal bleeding Postcoital bleeding Other / general Pelvic congestion syndrome Pelvic inflammatory disease External Vulva Bartholin's cyst Kraurosis vulvae Vestibular papillomatosis Vulvitis Vulvodynia Clitoral hood or clitoris Persistent genital arousal disorder
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Tree Nut Allergy
Wikipedia
by Tana Parker-Pope at The New York Times (15 Dec 2008) v t e Allergic conditions Respiratory system Allergic rhinitis (hay fever) Asthma Hypersensitivity pneumonitis Eosinophilic pneumonia Eosinophilic granulomatosis with polyangiitis Allergic bronchopulmonary aspergillosis Farmer's lung Laboratory animal allergy Skin Angioedema Urticaria Atopic dermatitis Allergic contact dermatitis Hypersensitivity vasculitis Blood and immune system Serum sickness Circulatory system Anaphylaxis Digestive system Coeliac disease Eosinophilic gastroenteritis Eosinophilic esophagitis Food allergy Egg allergy Milk intolerance Nervous system Eosinophilic meningitis Genitourinary system Acute interstitial nephritis Other conditions Drug allergy Allergic conjunctivitis Latex allergy v t e Hypersensitivity and autoimmune diseases Type I / allergy / atopy ( IgE ) Foreign Atopic eczema Allergic urticaria Allergic rhinitis (Hay fever) Allergic asthma Anaphylaxis Food allergy common allergies include: Milk Egg Peanut Tree nut Seafood Soy Wheat Penicillin allergy Autoimmune Eosinophilic esophagitis Type II / ADCC IgM IgG Foreign Hemolytic disease of the newborn Autoimmune Cytotoxic Autoimmune hemolytic anemia Immune thrombocytopenic purpura Bullous pemphigoid Pemphigus vulgaris Rheumatic fever Goodpasture syndrome Guillain–Barré syndrome " Type V "/ receptor Graves' disease Myasthenia gravis Pernicious anemia Type III ( Immune complex ) Foreign Henoch–Schönlein purpura Hypersensitivity vasculitis Reactive arthritis Farmer's lung Post-streptococcal glomerulonephritis Serum sickness Arthus reaction Autoimmune Systemic lupus erythematosus Subacute bacterial endocarditis Rheumatoid arthritis Type IV / cell-mediated ( T cells ) Foreign Allergic contact dermatitis Mantoux test Autoimmune Diabetes mellitus type 1 Hashimoto's thyroiditis Multiple sclerosis Coeliac disease Giant-cell arteritis Postorgasmic illness syndrome Reactive arthritis GVHD Transfusion-associated graft versus host disease Unknown/ multiple Foreign Hypersensitivity pneumonitis Allergic bronchopulmonary aspergillosis Transplant rejection Latex allergy (I+IV) Autoimmune Sjögren syndrome Autoimmune hepatitis Autoimmune polyendocrine syndrome APS1 APS2 Autoimmune adrenalitis Systemic autoimmune disease
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Spastic Paraplegia 11
Gene_reviews
Frequent clinical findings Progressive spasticity and weakness of the lower limbs Mild intellectual disability with learning difficulties in childhood and/or progressive cognitive decline with onset in the first to third decade Axonal, motor, or sensorimotor peripheral neuropathy (>80% of individuals) [Stevanin et al 2008, Orlacchio et al 2010, Daoud et al 2012, Özoğuz et al 2015, Manole et al 2016, Montecchiani et al 2016] Pseudobulbar involvement with dysarthria and/or dysphagia Increased reflexes in the upper limbs Less frequent clinical findings Cerebellar signs (ataxia or ocular signs including nystagmus and/or saccadic pursuit) Retinal degeneration (Kjellin syndrome) * [Puech et al 2011] Pes cavus Scoliosis Extrapyramidal signs such as parkinsonism [Anheim et al 2009, Faber et al 2018a] * Kjellin syndrome is characterized by retinal degeneration, autosomal recessive hereditary spastic paraplegia, and thin corpus callosum initially associated with spastic paraplegia 15 (SPG15) but more often occurring in individuals with SPG11. ... Eye findings can include the following: Macular excavation or degeneration as reported in the Kjellin syndrome [Orlén et al 2009, Puech et al 2011] Strabismus Cerebellar ocular signs such as abnormal saccadic pursuit and nystagmus in individuals with the longest disease duration Visual evoked potentials with increased latencies and decreased amplitudes [Stevanin et al 2008] Additional features are severe weakness, dysarthria, distal or generalized muscle wasting, and less frequently, pes cavus , scoliosis, parkinsonism, epilepsy, and orthostatic hypotension [Kara et al 2016]. ... Other Hereditary Spastic Paraplegias Associated with Thin Corpus Callosum (HSP-TCC) and Mental Impairment of Interest in the Differential Diagnosis of Spastic Paraplegia 11 (SPG11) View in own window Gene(s) Disorder 1 MOI Clinical Features of Differential Diagnosis Disorder Overlapping w/SPG11 Distinguishing from SPG11 AP4B1 SPG47 AR Seizures; white matter abnormalities Severe ID; facial dysmorphism; microcephaly; stereotypic laughter w/tongue protrusion AP4M1 SPG50 AP4E1 SPG51 AP4S1 SPG52 DDHD2 SPG54 AR Leukodystrophy Severe DD ERLIN2 SPG18 AR Also assoc w/epilepsy; DD Agenesis of corpus callosum SPG21 SPG21 (Mast syndrome) AR Late onset ataxia; adult-onset dementia & parkinsonism; polyneuropathy Japanese & Amish origin; akinetic mutism seen in advanced disease; psychiatric disease GBA2 SPG46 AR TCC; cerebellar &cerebral atrophy; DD; cerebellar signs; polyneuropathy Congenital cataract; male infertility (hypogonadism) TECPR2 SPG49 AR TCC reported occasionally Central apnea; severe DD; microcephaly; dysmorphic features; gastroesophageal reflux ZFYVE26 SPG15 AR DD; optic atrophy; ataxia; central retinal degeneration; polyneuropathy No clinical features discriminate between SPG11 & SPG15.
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Vps13d Movement Disorder
Gene_reviews
Imaging findings can resemble those seen in Leigh syndrome. Some individuals with VPS13D movement disorder have had normal brain MRI examinations. ... Imaging findings can resemble those seen in Leigh syndrome. Some individuals with VPS13D movement disorder have had normal brain MRI. ... Disorders to Consider in the Differential Diagnosis of VPS13D Movement Disorder View in own window Disorder Gene(s) MOI Clinical Features of the Differential Diagnosis Disorder Overlapping w/ VPS13D movement disorder Distinguishing from VPS13D movement disorder Spastic ataxia 1 1 VAMP1 AD Spastic ataxic gait Adult onset No dystonia Normal brain MRI Spastic ataxia 2 1 KIF1C AR Pediatric-onset spastic ataxic gait No extrapyramidal involvement Spastic ataxia 3 1 MARS2 AR Spastic ataxic gait White matter abnormalities Hearing impairment Spastic ataxia 4 1 MTPAP AR Spastic ataxia Neuropathy w/loss of reflexes Spastic ataxia 5 1 AFG3L2 AR Pediatric-onset spastic ataxia Dystonia Myoclonic epilepsy Oculomotor apraxia Leigh syndrome 2 Many AR XL mt Bilateral basal ganglia lesions Cardiac or skeletal muscle involvement HSP (incl SPG3A, SPG4, SPG7, SPG11) 3 ATL1 SPAST SPG7 SPG11 AD AR Pediatric-onset spastic gait No cerebellar features SCAR2 1 PMPCA AR Pediatric-onset ataxic gait Cerebellar atrophy SCAR7 1 TPP1 AR Pediatric-onset ataxic gait Posterior column involvement AD = autosomal dominant; AR = autosomal recessive; HSP = hereditary spastic paraplegia; MOI = mode of inheritance; mt = mitochondrial SCAR = spinocerebellar ataxia, autosomal recessive; XL = X-linked 1. ... See Mitochondrial DNA-Associated Leigh Syndrome and NARP. 3. These are the more common subtypes of hereditary spastic paraplegia with onset in childhood.ATXN1, ATXN7, CACNA1A, ATXN2, PRKCG, STUB1, PPP2R2B, SPTBN2, AFG3L2, TTBK2, TGM6, GRM1, CACNA1G, WWOX, ANO10, ATXN1L, CCDC88C, SYT14, TDP2, SNX14, GRID2, UBA5, SCYL1, NOP56, MME, TRPC3, CIC, CWF19L1, GFI1, RBM17, ELOVL5, RUBCN, VWA3B, FOXC1, POLG, PEX6, ATXN3, LY6E, PNPLA6, TDP1, ITPR1, TWNK, TBP, SLC52A2, FXN, ATN1, ATXN8OS, ATXN10, CASP3, KCND3, TPO, CANT1, PLEKHG4, APTX, SPG7, HTT, FMR1, FGF14, C9orf72, PDYN, KCNC3, TTPA, JPH3, COQ8A, CAPN1, PRNP, CNTN4, AR, AIPL1, SETX, TREH, CDK20, RAI1, MTCL1, PNKP, NFAT5, ALAS2, FGF20, FGF21, FMR1-IT1, AAA1, MIR29A, MIR144, NUP43, TMEM240, SUMF1, NEAT1, SCASI, BEAN1, LRRK2, OGA, PAG1, VPS13D, TTC19, COQ4, COQ2, PCBP4, TGFB1, PRPF8, FGF8, KCNA1, IGFALS, HLA-A, H2AX, GUCA1A, GLO1, GJB1, GFAP, FRAXE, FRAXA, FGF10, FGF9, FGF3, PUM1, F13A1, ETV1, EPHB2, ELF2, EIF4E, CRH, CREBBP, CAT, KIF1A, ATP2B3, APP, APOE, LIG4, ATP6, NEFL, PRKN, ERDA1, CDKL1, PLA2G6, AAAS, FGF23, UCHL3, TRIO, TOP1, TK2, TH, ABCD1, TCF4, ELOVL4, ST8, SOD1, SNCA, SCN8A, RPS4X, RPE65, OPN1LW, PSMC6, MAPK1, PRKACG, PLA2G2A, PLA2G1B, H3P30
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Photosensitive Epilepsy
Wikipedia
External links [ edit ] HardingFPA Broadcast Flash and Pattern Analyser Photosensitive+Epilepsy at the US National Library of Medicine Medical Subject Headings (MeSH) v t e Seizures and epilepsy Basics Seizure types Aura (warning sign) Postictal state Epileptogenesis Neonatal seizure Epilepsy in children Management Anticonvulsants Investigations Electroencephalography Epileptologist Personal issues Epilepsy and driving Epilepsy and employment Seizure types Focal Seizures Simple partial Complex partial Gelastic seizure Epilepsy Temporal lobe epilepsy Frontal lobe epilepsy Rolandic epilepsy Nocturnal epilepsy Panayiotopoulos syndrome Vertiginous epilepsy Generalised Tonic–clonic Absence seizure Atonic seizure Automatism Benign familial neonatal seizures Lennox–Gastaut syndrome Myoclonic astatic epilepsy Epileptic spasms Status epilepticus Epilepsia partialis continua Complex partial status epilepticus Myoclonic epilepsy Progressive myoclonus epilepsy Dentatorubral–pallidoluysian atrophy Unverricht–Lundborg disease MERRF syndrome Lafora disease Juvenile myoclonic epilepsy Non-epileptic seizure Febrile seizure Psychogenic non-epileptic seizure Related disorders Sudden unexpected death in epilepsy Todd's paresis Landau–Kleffner syndrome Epilepsy in animals Organizations Citizens United for Research in Epilepsy (US) Epilepsy Action (UK) Epilepsy Action Australia Epilepsy Foundation (US) Epilepsy Outlook (UK) Epilepsy Research UK Epilepsy Society (UK)
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Stress Fracture
Wikipedia
External links [ edit ] Classification D ICD - 10 : M48.4 , M84.3 ICD - 9-CM : 733.93 , 733.94 , 733.95 MeSH : D015775 DiseasesDB : 7842 External resources eMedicine : radio/783 orthped/446 pmr/134 v t e Bone and joint disease Bone Inflammation endocrine : Osteitis fibrosa cystica Brown tumor infection : Osteomyelitis Sequestrum Involucrum Sesamoiditis Brodie abscess Periostitis Vertebral osteomyelitis Metabolic Bone density Osteoporosis Juvenile Osteopenia Osteomalacia Paget's disease of bone Hypophosphatasia Bone resorption Osteolysis Hajdu–Cheney syndrome Ainhum Gorham's disease Other Ischaemia Avascular necrosis Osteonecrosis of the jaw Complex regional pain syndrome Hypertrophic pulmonary osteoarthropathy Nonossifying fibroma Pseudarthrosis Stress fracture Fibrous dysplasia Monostotic Polyostotic Skeletal fluorosis bone cyst Aneurysmal bone cyst Hyperostosis Infantile cortical hyperostosis Osteosclerosis Melorheostosis Pycnodysostosis Joint Chondritis Relapsing polychondritis Other Tietze's syndrome Combined Osteochondritis Osteochondritis dissecans Child leg: hip Legg–Calvé–Perthes syndrome tibia Osgood–Schlatter disease Blount's disease foot Köhler disease Sever's disease spine Scheuermann's_disease arm: wrist Kienböck's disease elbow Panner disease
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Roseola
Wikipedia
External links [ edit ] Classification D ICD - 10 : B08.2 ICD - 9-CM : 057.8 MeSH : D005077 DiseasesDB : 5857 SNOMED CT : 240559001 External resources MedlinePlus : 000968 eMedicine : emerg/400 derm/378 ped/998 DermNet viral/roseola v t e Skin infections , symptoms and signs related to viruses DNA virus Herpesviridae Alpha HSV Herpes simplex Herpetic whitlow Herpes gladiatorum Herpes simplex keratitis Herpetic sycosis Neonatal herpes simplex Herpes genitalis Herpes labialis Eczema herpeticum Herpetiform esophagitis Herpes B virus B virus infection VZV Chickenpox Herpes zoster Herpes zoster oticus Ophthalmic zoster Disseminated herpes zoster Zoster-associated pain Modified varicella-like syndrome Beta Human herpesvirus 6 / Roseolovirus Exanthema subitum Roseola vaccinia Cytomegalic inclusion disease Gamma KSHV Kaposi's sarcoma Poxviridae Ortho Variola Smallpox Alastrim MoxV Monkeypox CPXV Cowpox VV Vaccinia Generalized vaccinia Eczema vaccinatum Progressive vaccinia Buffalopox Para Farmyard pox : Milker's nodule Bovine papular stomatitis Pseudocowpox Orf Sealpox Other Yatapoxvirus : Tanapox Yaba monkey tumor virus MCV Molluscum contagiosum Papillomaviridae HPV Wart / plantar wart Heck's disease Genital wart giant Laryngeal papillomatosis Butcher's wart Bowenoid papulosis Epidermodysplasia verruciformis Verruca plana Pigmented wart Verrucae palmares et plantares BPV Equine sarcoid Parvoviridae Parvovirus B19 Erythema infectiosum Reticulocytopenia Papular purpuric gloves and socks syndrome Polyomaviridae Merkel cell polyomavirus Merkel cell carcinoma RNA virus Paramyxoviridae MeV Measles Togaviridae Rubella virus Rubella Congenital rubella syndrome ("German measles" ) Alphavirus infection Chikungunya fever Picornaviridae CAV Hand, foot, and mouth disease Herpangina FMDV Foot-and-mouth disease Boston exanthem disease Ungrouped Asymmetric periflexural exanthem of childhood Post-vaccination follicular eruption Lipschütz ulcer Eruptive pseudoangiomatosis Viral-associated trichodysplasia Gianotti–Crosti syndrome v t e Numbered Diseases of Childhood Diseases First Disease (Measles) Second Disease (Scarlet Fever) Third Disease (Rubella) Fourth Disease (Dukes' Disease) Fifth Disease (Erythema Infectiosum) Sixth Disease (Roseola)
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Anosognosia
Wikipedia
Recent studies from the empirical data are prone to consider anosognosia a multi-componential syndrome or multi-faceted phenomenon. That is it can be manifested by failure to be aware of a number of specific deficits, including motor ( hemiplegia ), sensory (hemianaesthesia, hemianopia ), spatial ( unilateral neglect ), memory ( dementia ), and language ( receptive aphasia ) due to impairment of anatomo-functionally discrete monitoring systems. [1] [2] Anosognosia is relatively common following different causes of brain injury, such as stroke and traumatic brain injury ; for example, anosognosia for hemiparesis (weakness of one side of the body) with onset of acute stroke is estimated at between 10% and 18%. [6] However, it can appear to occur in conjunction with virtually any neurological impairment. ... This phenomenon of double dissociation can be an indicator of domain-specific disorders of awareness modules, meaning that in anosognosia, brain damage can selectively impact the self-monitoring process of one specific physical or cognitive function rather than a spatial location of the body. [1] [2] [11] There are also studies showing that the maneuver of vestibular stimulation could temporarily improve both the syndrome of spatial unilateral neglect and of anosognosia for left hemiplegia. Combining the findings of hemispheric asymmetry to the right, association with spatial unilateral neglect, and the temporal improvement on both syndromes, it is suggested there can be a spatial component underlying the mechanism of anosognosia for motor weakness and that neural processes could be modulated similarly. [2] There were some cases of anosognosia for right hemiplegia after left hemisphere damage, but the frequency of this type of anosognosia has not been estimated. [1] Those diagnosed with Alzheimer's disease often display this lack of awareness and insist that nothing is wrong with them. ... Anosognosia is also closely related to other cognitive dysfunctions that may impair the capacity of an individual to continuously participate in treatment. [25] Other research has suggested that attitudes toward treatment can improve after involuntary treatment and that previously committed patients tend later to seek voluntary treatment. [26] See also [ edit ] Anosodiaphoria Anton–Babinski syndrome Brain damage Cerebral hypoxia Confabulation Cotard delusion Denial Depersonalization disorder Dunning–Kruger effect Egosyntonic Introspection illusion Oliver Sacks Unilateral neglect (also known as hemispatial neglect) References [ edit ] ^ a b c d e Moro, Valentina; Pernigo, Simone; Zapparoli, Paola; Cordioli, Zeno; Aglioti, Salvatore M. (2011).