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Flaccid Paralysis
Wikipedia
This is in contrast to an upper motor neuron lesion , which often presents with spasticity , although early on this may present with flaccid paralysis. [ citation needed ] Included in AFP's list are poliomyelitis (polio), transverse myelitis, Guillain–Barré syndrome , enteroviral encephalopathy, [7] traumatic neuritis, Reye's syndrome , etc. ... Retrieved 2014-02-26 . ^ Idris M, Elahi M, Arif A (Jan–Mar 2007). "Guillain Barre syndrome: the leading cause of acute flaccid paralysis in Hazara division". ... Centers for Disease Control and Prevention (CDC). "Acute flaccid paralysis syndrome associated with West Nile virus infection--Mississippi and Louisiana, July-August 2002". ... External links [ edit ] WHO Programme for Immunization Preventable Diseases (IPD) A Collaboration between World Health Organization and Government of Nepal Classification D ICD - 10 : G81.0 , G82.0 , G82.3 ICD - 9-CM : 359.9 Look up flaccid in Wiktionary, the free dictionary. v t e Symptoms and signs relating to movement and gait Gait Gait abnormality CNS Scissor gait Cerebellar ataxia Festinating gait Marche à petit pas Propulsive gait Stomping gait Spastic gait Magnetic gait Truncal ataxia Muscular Myopathic gait Trendelenburg gait Pigeon gait Steppage gait Antalgic gait Coordination Ataxia Cerebellar ataxia Dysmetria Dysdiadochokinesia Pronator drift Dyssynergia Sensory ataxia Asterixis Abnormal movement Athetosis Tremor Fasciculation Fibrillation Posturing Abnormal posturing Opisthotonus Spasm Trismus Cramp Tetany Myokymia Joint locking Paralysis Flaccid paralysis Spastic paraplegia Spastic diplegia Spastic paraplegia Syndromes Monoplegia Diplegia / Paraplegia Hemiplegia Triplegia Tetraplegia / Quadruplegia General causes Upper motor neuron lesion Lower motor neuron lesion Weakness Hemiparesis Other Rachitic rosary Hyperreflexia Clasp-knife response
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Carnosinemia
Wikipedia
External links [ edit ] Classification D ICD - 10 : E70.8 ICD - 9-CM : 270.5 OMIM : 212200 DiseasesDB : 29672 SNOMED CT : 410052008 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
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Postpartum Thyroiditis
Wikipedia
Endocrinology & Metabolism Clinics of North America , 29(2), 417–430. doi : 10.1016/S0889-8529(05)70140-7 Classification D ICD - 10 : O90.5 MeSH : D050032 DiseasesDB : 10441 SNOMED CT : 52772002 v t e Thyroid disease Hypothyroidism Iodine deficiency Cretinism Congenital hypothyroidism Myxedema Myxedema coma Euthyroid sick syndrome Signs and symptoms Queen Anne's sign Woltman sign Thyroid dyshormonogenesis Pickardt syndrome Hyperthyroidism Hyperthyroxinemia Thyroid hormone resistance Familial dysalbuminemic hyperthyroxinemia Hashitoxicosis Thyrotoxicosis factitia Thyroid storm Graves' disease Signs and symptoms Abadie's sign of exophthalmic goiter Boston's sign Dalrymple's sign Stellwag's sign lid lag Griffith's sign Möbius sign Pretibial myxedema Graves' ophthalmopathy Thyroiditis Acute infectious Subacute De Quervain's Subacute lymphocytic Palpation Autoimmune /chronic Hashimoto's Postpartum Riedel's Enlargement Goitre Endemic goitre Toxic nodular goitre Toxic multinodular goiter Thyroid nodule Colloid nodule v t e Pathology of pregnancy , childbirth and the puerperium Pregnancy Pregnancy with abortive outcome Abortion Ectopic pregnancy Abdominal Cervical Interstitial Ovarian Heterotopic Embryo loss Fetal resorption Molar pregnancy Miscarriage Stillbirth Oedema , proteinuria and hypertensive disorders Gestational hypertension Pre-eclampsia HELLP syndrome Eclampsia Other, predominantly related to pregnancy Digestive system Acute fatty liver of pregnancy Gestational diabetes Hepatitis E Hyperemesis gravidarum Intrahepatic cholestasis of pregnancy Integumentary system / dermatoses of pregnancy Gestational pemphigoid Impetigo herpetiformis Intrahepatic cholestasis of pregnancy Linea nigra Prurigo gestationis Pruritic folliculitis of pregnancy Pruritic urticarial papules and plaques of pregnancy (PUPPP) Striae gravidarum Nervous system Chorea gravidarum Blood Gestational thrombocytopenia Pregnancy-induced hypercoagulability Maternal care related to the fetus and amniotic cavity amniotic fluid Oligohydramnios Polyhydramnios Braxton Hicks contractions chorion / amnion Amniotic band syndrome Chorioamnionitis Chorionic hematoma Monoamniotic twins Premature rupture of membranes Obstetrical bleeding Antepartum placenta Circumvallate placenta Monochorionic twins Placenta accreta Placenta praevia Placental abruption Twin-to-twin transfusion syndrome Labor Amniotic fluid embolism Cephalopelvic disproportion Dystocia Shoulder dystocia Fetal distress Locked twins Nuchal cord Obstetrical bleeding Postpartum Pain management during childbirth placenta Placenta accreta Preterm birth Postmature birth Umbilical cord prolapse Uterine inversion Uterine rupture Vasa praevia Puerperal Breastfeeding difficulties Low milk supply Cracked nipples Breast engorgement Childbirth-related posttraumatic stress disorder Diastasis symphysis pubis Postpartum bleeding Peripartum cardiomyopathy Postpartum depression Postpartum psychosis Postpartum thyroiditis Puerperal fever Puerperal mastitis Other Concomitant conditions Diabetes mellitus Systemic lupus erythematosus Thyroid disorders Maternal death Sexual activity during pregnancy Category “Postpartum Thyroiditis.”
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Splenic Infarction
Wikipedia
Splenectomy may be warranted for persistent pseudocysts due to the high risk of subsequent rupture. [8] Contents 1 Causes 1.1 Therapeutic infarction 2 References 3 External links Causes [ edit ] Splenic infarct seen on CT Healed splenic infarct Several factors may increase the tendency for clot formation , such as specific infections (such as infectious mononucleosis , [9] [ dubious – discuss ] [ better source needed ] cytomegalovirus infection , [10] malaria , [11] or babesiosis [12] ), inherited clotting disorders ( thrombophilia , such as Factor V Leiden , antiphospholipid syndrome ), malignancy (such as pancreatic cancer ) or metastasis , or a combination [13] of these factors. ... And among them, 5 of 9 hitherto silent antiphospholipid syndrome or mitral valve disease had been identified. [18] Two remained cryptogenic . [18] Therapeutic infarction [ edit ] Splenic infarction can be induced for the treatment of such conditions as portal hypertension or splenic injury . [19] It can also be used prior to splenectomy for the prevention of blood loss . ... External links [ edit ] Classification D ICD - 10 : D73.5 MeSH : D013159 DiseasesDB : 12365 External resources MedlinePlus : 001293 eMedicine : article/193718 v t e Ischaemia and infarction Ischemia Location Brain ischemia Heart Large intestine Small intestine Infarction Types Anemic Hemorrhagic Location Heart Brain Spleen Limb Gangrene v t e Lymphatic disease : organ and vessel diseases Thymus Abscess Hyperplasia Hypoplasia DiGeorge syndrome Ectopic thymus Thymoma Thymic carcinoma Spleen Asplenia Asplenia with cardiovascular anomalies Accessory spleen Polysplenia Wandering spleen Splenomegaly Banti's syndrome Splenic infarction Splenic tumor Lymph node Lymphadenopathy Generalized lymphadenopathy Castleman's disease Intranodal palisaded myofibroblastoma Kikuchi disease Tonsils see Template:Respiratory pathology Lymphatic vessels Lymphangitis Lymphangiectasia Lymphedema Primary lymphedema Congenital lymphedema Lymphedema praecox Lymphedema tarda Lymphedema–distichiasis syndrome Milroy's disease Secondary lymphedema Bullous lymphedema Factitial lymphedema Postinflammatory lymphedema Postmastectomy lymphangiosarcoma Waldmann disease
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Bone Cyst
Wikipedia
External links [ edit ] Classification D MeSH : D001845 SNOMED CT : 203465002 v t e Acquired tooth disease Hard tissues Caries (tooth decay) Attrition Abrasion Erosion Hypercementosis tooth resorption ( External resorption , Internal resorption , Root resorption ) Pulp/periapical ( Endodontal ) Pulpal External resorption Internal resorption Irreversible pulpitis Reversible pulpitis Pulp necrosis Pink tooth of Mummery Periapical Acute apical periodontitis Chronic apical periodontitis Combined periodontic-endodontic lesions Fistula Periapical abscess Phoenix abscess Vertical root fracture Ungrouped Pulpitis Radicular cyst Periapical abscess Gingiva/periodontal ( Periodontal ) Gingivitis Periodontitis ( Chronic periodontitis ) Periodontal disease Bone cyst Dentigerous cyst Calcifying odontogenic cyst Glandular odontogenic cyst Other Cracked tooth syndrome To be grouped from periodontology Diagnoses Chronic periodontitis Localized aggressive periodontitis Generalized aggressive periodontitis Periodontitis as a manifestation of systemic disease Necrotizing periodontal diseases Abscesses of the periodontium Combined periodontic-endodontic lesions Pathogenesis A. actinomycetemcomitans Capnocytophaga sp. F. nucleatum P. gingivalis P. intermedia T. forsythia T. denticola Pathologic entities Calculus Edentulism Fremitus Furcation defect Gingival enlargement Gingival pocket Gingivitis Horizontal bony defect Linear gingival erythema Occlusal trauma Periodontal pocket Periodontal disease Periodontitis Plaque Recession Vertical bony defect 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 Authority control GND : 4164305-7
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Lichen Nitidus
Wikipedia
External links [ edit ] Classification D ICD - 10 : L44.1 ICD - 9-CM : 697.1 MeSH : D017513 DiseasesDB : 34283 External resources eMedicine : derm/232 Lichen Nitidus at DermNet photo library v t e Diseases of the skin and appendages by morphology Growths Epidermal Wart Callus Seborrheic keratosis Acrochordon Molluscum contagiosum Actinic keratosis Squamous-cell carcinoma Basal-cell carcinoma Merkel-cell carcinoma Nevus sebaceous Trichoepithelioma Pigmented Freckles Lentigo Melasma Nevus Melanoma Dermal and subcutaneous Epidermal inclusion cyst Hemangioma Dermatofibroma (benign fibrous histiocytoma) Keloid Lipoma Neurofibroma Xanthoma Kaposi's sarcoma Infantile digital fibromatosis Granular cell tumor Leiomyoma Lymphangioma circumscriptum Myxoid cyst Rashes With epidermal involvement Eczematous Contact dermatitis Atopic dermatitis Seborrheic dermatitis Stasis dermatitis Lichen simplex chronicus Darier's disease Glucagonoma syndrome Langerhans cell histiocytosis Lichen sclerosus Pemphigus foliaceus Wiskott–Aldrich syndrome Zinc deficiency Scaling Psoriasis Tinea ( Corporis Cruris Pedis Manuum Faciei ) Pityriasis rosea Secondary syphilis Mycosis fungoides Systemic lupus erythematosus Pityriasis rubra pilaris Parapsoriasis Ichthyosis Blistering Herpes simplex Herpes zoster Varicella Bullous impetigo Acute contact dermatitis Pemphigus vulgaris Bullous pemphigoid Dermatitis herpetiformis Porphyria cutanea tarda Epidermolysis bullosa simplex Papular Scabies Insect bite reactions Lichen planus Miliaria Keratosis pilaris Lichen spinulosus Transient acantholytic dermatosis Lichen nitidus Pityriasis lichenoides et varioliformis acuta Pustular Acne vulgaris Acne rosacea Folliculitis Impetigo Candidiasis Gonococcemia Dermatophyte Coccidioidomycosis Subcorneal pustular dermatosis Hypopigmented Tinea versicolor Vitiligo Pityriasis alba Postinflammatory hyperpigmentation Tuberous sclerosis Idiopathic guttate hypomelanosis Leprosy Hypopigmented mycosis fungoides Without epidermal involvement Red Blanchable Erythema Generalized Drug eruptions Viral exanthems Toxic erythema Systemic lupus erythematosus Localized Cellulitis Abscess Boil Erythema nodosum Carcinoid syndrome Fixed drug eruption Specialized Urticaria Erythema ( Multiforme Migrans Gyratum repens Annulare centrifugum Ab igne ) Nonblanchable Purpura Macular Thrombocytopenic purpura Actinic/solar purpura Papular Disseminated intravascular coagulation Vasculitis Indurated Scleroderma / morphea Granuloma annulare Lichen sclerosis et atrophicus Necrobiosis lipoidica Miscellaneous disorders Ulcers Hair Telogen effluvium Androgenic alopecia Alopecia areata Systemic lupus erythematosus Tinea capitis Loose anagen syndrome Lichen planopilaris Folliculitis decalvans Acne keloidalis nuchae Nail Onychomycosis Psoriasis Paronychia Ingrown nail Mucous membrane Aphthous stomatitis Oral candidiasis Lichen planus Leukoplakia Pemphigus vulgaris Mucous membrane pemphigoid Cicatricial pemphigoid Herpesvirus Coxsackievirus Syphilis Systemic histoplasmosis Squamous-cell carcinoma v t e Papulosquamous disorders Psoriasis Pustular Generalized pustular psoriasis ( Impetigo herpetiformis ) Acropustulosis / Pustulosis palmaris et plantaris ( Pustular bacterid ) Annular pustular psoriasis Localized pustular psoriasis Other Guttate psoriasis Psoriatic arthritis Psoriatic erythroderma Drug-induced psoriasis Inverse psoriasis Napkin psoriasis Seborrheic-like psoriasis Parapsoriasis Pityriasis lichenoides ( Pityriasis lichenoides et varioliformis acuta , Pityriasis lichenoides chronica ) Lymphomatoid papulosis Small plaque parapsoriasis ( Digitate dermatosis , Xanthoerythrodermia perstans ) Large plaque parapsoriasis ( Retiform parapsoriasis ) Other pityriasis Pityriasis rosea Pityriasis rubra pilaris Pityriasis rotunda Pityriasis amiantacea Other lichenoid Lichen planus configuration Annular Linear morphology Hypertrophic Atrophic Bullous Ulcerative Actinic Pigmented site Mucosal Nails Peno-ginival Vulvovaginal overlap synromes with lichen sclerosus with lupus erythematosis other: Hepatitis-associated lichen planus Lichen planus pemphigoides Other Lichen nitidus Lichen striatus Lichen ruber moniliformis Gianotti–Crosti syndrome Erythema dyschromicum perstans Idiopathic eruptive macular pigmentation Keratosis lichenoides chronica Kraurosis vulvae Lichen sclerosus Lichenoid dermatitis Lichenoid reaction of graft-versus-host disease
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Lupus And Pregnancy
Wikipedia
The overall live-birth rate in somebody with lupus has been estimated to be 72%. [5] Pregnancy outcome appears to be worse in those with lupus whose disease flares up during pregnancy. [6] Miscarriages in the first trimester appear either to have no known cause or to be associated with signs of active lupus. [7] Later losses appear to occur primarily due to the antiphospholipid syndrome , in spite of treatment with heparin and aspirin . [7] All women with lupus, even those without previous history of miscarriage, are recommended to be screened for antiphospholipid antibodies , both the lupus anticoagulant (the RVVT and sensitive PTT are the best screening battery) and anticardiolipin antibodies . [7] Neonatal lupus [ edit ] Neonatal lupus is the occurrence of lupus symptoms in an infant born from a mother with lupus, most commonly presenting with a rash resembling discoid lupus erythematosus , and sometimes with systemic abnormalities such as heart block or hepatosplenomegaly . [8] Neonatal lupus is usually benign and self-limited. [8] Still, identification of mothers at highest risk for complications allows for prompt treatment before or after birth. ... For example, chloasma may appear like the malar rash of lupus, proteinuria from preeclampsia may appear like that of lupus nephritis , thrombocytopenia of the HELLP syndrome may appear like that of lupus, and pregnancy-related edema of joints can appear like arthritis of lupus. [2] General preventive measures [ edit ] Continuing glucocorticoids at the lowest effective dose and/or cautious use of azathioprine may be preferred in some patients, but needs to be weighed against potential adverse effects of such medications. [2] References [ edit ] ^ "Planning a pregnancy when you have lupus | Lupus Foundation of America" . www.lupus.org . ... Chief Editor: David Chelmow. [1] v t e Pregnancy and childbirth Planning Birth control Natural family planning Pre-conception counseling Conception Assisted reproductive technology Artificial insemination Fertility medication In vitro fertilisation Fertility awareness Unintended pregnancy Testing 3D ultrasound Obstetric ultrasonography Pregnancy test Home testing Prenatal diagnosis Prenatal Anatomy Amniotic fluid Amniotic sac Endometrium Placenta Development Fundal height Gestational age Human embryogenesis Maternal physiological changes Postpartum physiological changes Care Nutrition Environmental toxicants In pregnancy Prenatal Concomitant conditions Drinking Diabetes mellitus Smoking Vaping SLE Sexual activity during pregnancy Procedures Amniocentesis Cardiotocography Chorionic villus sampling Nonstress test Abortion Childbirth Preparation Bradley method Hypnobirthing Lamaze Nesting instinct Roles Doula Birth attendant Men's roles Midwife Obstetrician Perinatal nurse Traditional birth attendant Delivery Bloody show Childbirth positions Home birth Multiple birth Natural childbirth Pelvimetry / Bishop score Cervical dilation Cervical effacement Position Presentation Breech Cephalic Shoulder Rupture of membranes Unassisted childbirth Uterine contraction Water birth Postpartum Maternal Postpartum confinement Sex after pregnancy Psychiatric disorders of childbirth Postpartum physiological changes Roles Doula Health visitor Lactation consultant Monthly nurse Confinement nanny Infant Adaptation to extrauterine life Child care Congenital disorders Obstetric history Gravidity and parity v t e Pathology of pregnancy , childbirth and the puerperium Pregnancy Pregnancy with abortive outcome Abortion Ectopic pregnancy Abdominal Cervical Interstitial Ovarian Heterotopic Embryo loss Fetal resorption Molar pregnancy Miscarriage Stillbirth Oedema , proteinuria and hypertensive disorders Gestational hypertension Pre-eclampsia HELLP syndrome Eclampsia Other, predominantly related to pregnancy Digestive system Acute fatty liver of pregnancy Gestational diabetes Hepatitis E Hyperemesis gravidarum Intrahepatic cholestasis of pregnancy Integumentary system / dermatoses of pregnancy Gestational pemphigoid Impetigo herpetiformis Intrahepatic cholestasis of pregnancy Linea nigra Prurigo gestationis Pruritic folliculitis of pregnancy Pruritic urticarial papules and plaques of pregnancy (PUPPP) Striae gravidarum Nervous system Chorea gravidarum Blood Gestational thrombocytopenia Pregnancy-induced hypercoagulability Maternal care related to the fetus and amniotic cavity amniotic fluid Oligohydramnios Polyhydramnios Braxton Hicks contractions chorion / amnion Amniotic band syndrome Chorioamnionitis Chorionic hematoma Monoamniotic twins Premature rupture of membranes Obstetrical bleeding Antepartum placenta Circumvallate placenta Monochorionic twins Placenta accreta Placenta praevia Placental abruption Twin-to-twin transfusion syndrome Labor Amniotic fluid embolism Cephalopelvic disproportion Dystocia Shoulder dystocia Fetal distress Locked twins Nuchal cord Obstetrical bleeding Postpartum Pain management during childbirth placenta Placenta accreta Preterm birth Postmature birth Umbilical cord prolapse Uterine inversion Uterine rupture Vasa praevia Puerperal Breastfeeding difficulties Low milk supply Cracked nipples Breast engorgement Childbirth-related posttraumatic stress disorder Diastasis symphysis pubis Postpartum bleeding Peripartum cardiomyopathy Postpartum depression Postpartum psychosis Postpartum thyroiditis Puerperal fever Puerperal mastitis Other Concomitant conditions Diabetes mellitus Systemic lupus erythematosus Thyroid disorders Maternal death Sexual activity during pregnancy Category
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Esophageal Dysphagia
Wikipedia
Esophageal stricture can also be due to other causes, such as acid reflux from Zollinger–Ellison syndrome , trauma from a nasogastric tube placement, and chronic acid exposure in patients with poor esophageal motility from scleroderma. ... An important association of esophageal webs is to the Plummer–Vinson syndrome in iron deficiency , in which case patients will also have anemia, koilonychia, fatigue, and other symptoms of anemia . ... The combination of achalasia, adrenal insufficiency, and alacrima (lack of tear production) in children is known as the triple-A (Allgrove) syndrome . In most cases the cause is unknown (idiopathic), but in some regions of the world, achalasia can also be caused by Chagas disease due to infection by Trypanosoma cruzi . ... External links [ edit ] Classification D ICD - 10 : R13 ICD - 9-CM : 787.24 MeSH : D003680 DiseasesDB : 17942 External resources MedlinePlus : 003115 eMedicine : pmr/194 v t e Symptoms and signs relating to the human digestive system or abdomen Gastrointestinal tract Nausea Vomiting Heartburn Aerophagia Pagophagia Dysphagia oropharyngeal esophageal Odynophagia Bad breath Xerostomia Hypersalivation Burping Wet burp Goodsall's rule Chilaiditi syndrome Dance's sign Aaron's sign Arapov's sign Markle sign McBurney's point Sherren's triangle Radiologic signs : Hampton's line Klemm's sign Accessory liver : Councilman body Mallory body biliary: Boas' sign Courvoisier's law Charcot's cholangitis triad / Reynolds' pentad cholecystitis ( Murphy's sign Lépine's sign Mirizzi's syndrome ) Nardi test Defecation Flatulence Fecal incontinence Encopresis Fecal occult blood Rectal tenesmus Constipation Obstructed defecation Diarrhea Rectal discharge Psoas sign Obturator sign Rovsing's sign Hamburger sign Heel tap sign Aure-Rozanova's sign Dunphy sign Alder's sign Lockwood's sign Rosenstein's sign Abdomen Pain Abdominal pain Acute abdomen Colic Baby colic Abdominal guarding Blumberg sign Distension Abdominal distension Bloating Ascites Tympanites Shifting dullness Ascites Fluid wave test Masses Abdominal mass Hepatosplenomegaly Hepatomegaly Splenomegaly Other Jaundice Mallet-Guy sign Puddle sign Ballance's sign Aortic insufficiency Castell's sign Kehr's sign Cullen's sign Grey Turner's sign Hernia Howship–Romberg sign Hannington-Kiff sign Other Cupola sign Fothergill's sign Carnett's sign Sister Mary Joseph nodule
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Fournier Gangrene
Wikipedia
v t e Male diseases of the pelvis and genitals Internal Testicular Orchitis Hydrocele testis Testicular cancer Testicular torsion Male infertility Aspermia Asthenozoospermia Azoospermia Hyperspermia Hypospermia Oligospermia Necrospermia Teratospermia Epididymis Epididymitis Spermatocele Hematocele Prostate Prostatitis Acute prostatitis Chronic bacterial prostatitis Chronic prostatitis/chronic pelvic pain syndrome Asymptomatic inflammatory prostatitis Benign prostatic hyperplasia Prostate cancer Seminal vesicle Seminal vesiculitis External Penis Balanoposthitis / Balanitis Balanitis plasmacellularis Pseudoepitheliomatous keratotic and micaceous balanitis Phimosis Paraphimosis Priapism Sexual dysfunction Erectile dysfunction Peyronie's disease Penile cancer Penile fracture Balanitis xerotica obliterans Other Hematospermia Retrograde ejaculation Postorgasmic illness syndrome 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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Omsk Hemorrhagic Fever
Wikipedia
J Med Virol doi: 10.1002/jmv.23856 External links [ edit ] Classification D ICD - 10 : A98.1 ICD - 9-CM : 065.1 MeSH : D006481 DiseasesDB : 31095 External resources Orphanet : 319266 https://www.cdc.gov/ncidod/dvrd/spb/mnpages/dispages/omsk.htm 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 : Q18417346 EoL : 541214 IRMNG : 11460384 NCBI : 12542
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Tyrosinemia
Wikipedia
External links [ edit ] Classification D ICD - 10 : E70.2 ICD - 9-CM : 270.2 OMIM : 276700 276600 276710 MeSH : D020176 DiseasesDB : 13478 External resources eMedicine : ped/2339 Patient UK : Tyrosinemia GeneReview/NCBI/NIH/UW entry on Tyrosinemia Type 1 Tyrosinemia on Genetic Home Reference 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 v t e Medicine Specialties and subspecialties Surgery Cardiac surgery Cardiothoracic surgery Colorectal surgery Eye surgery General surgery Neurosurgery Oral and maxillofacial surgery Orthopedic surgery Hand surgery Otolaryngology ENT Pediatric surgery Plastic surgery Reproductive surgery Surgical oncology Transplant surgery Trauma surgery Urology Andrology Vascular surgery Internal medicine Allergy / Immunology Angiology Cardiology Endocrinology Gastroenterology Hepatology Geriatrics Hematology Hospital medicine Infectious disease Nephrology Oncology Pulmonology Rheumatology Obstetrics and gynaecology Gynaecology Gynecologic oncology Maternal–fetal medicine Obstetrics Reproductive endocrinology and infertility Urogynecology Diagnostic Radiology Interventional radiology Nuclear medicine Pathology Anatomical Clinical pathology Clinical chemistry Cytopathology Medical microbiology Transfusion medicine Other Addiction medicine Adolescent medicine Anesthesiology Dermatology Disaster medicine Diving medicine Emergency medicine Mass gathering medicine Family medicine General practice Hospital medicine Intensive care medicine Medical genetics Narcology Neurology Clinical neurophysiology Occupational medicine Ophthalmology Oral medicine Pain management Palliative care Pediatrics Neonatology Physical medicine and rehabilitation PM&R Preventive medicine Psychiatry Addiction psychiatry Radiation oncology Reproductive medicine Sexual medicine Sleep medicine Sports medicine Transplantation medicine Tropical medicine Travel medicine Venereology Medical education Medical school Bachelor of Medicine, Bachelor of Surgery Bachelor of Medical Sciences Master of Medicine Master of Surgery Doctor of Medicine Doctor of Osteopathic Medicine MD–PhD Related topics Alternative medicine Allied health Dentistry Podiatry Pharmacy Physiotherapy Molecular oncology Nanomedicine Personalized medicine Public health Rural health Therapy Traditional medicine Veterinary medicine Physician Chief physician History of medicine Book Category Commons Wikiproject Portal Outline
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Intermittent Claudication
Wikipedia
External links [ edit ] Classification D ICD - 10 : I73.9 ICD - 9-CM : 440.21 MeSH : D007383 Cochrane Peripheral Vascular Diseases Review Group QUANTAFLO Peripheral Arterial Disease Test v t e Cardiovascular disease (vessels) Arteries , arterioles and capillaries Inflammation Arteritis Aortitis Buerger's disease Peripheral artery disease Arteriosclerosis Atherosclerosis Foam cell Fatty streak Atheroma Intermittent claudication Critical limb ischemia Monckeberg's arteriosclerosis Arteriolosclerosis Hyaline Hyperplastic Cholesterol LDL Oxycholesterol Trans fat Stenosis Carotid artery stenosis Renal artery stenosis Other Aortoiliac occlusive disease Degos disease Erythromelalgia Fibromuscular dysplasia Raynaud's phenomenon Aneurysm / dissection / pseudoaneurysm torso : Aortic aneurysm Abdominal aortic aneurysm Thoracic aortic aneurysm Aneurysm of sinus of Valsalva Aortic dissection Aortic rupture Coronary artery aneurysm head / neck Intracranial aneurysm Intracranial berry aneurysm Carotid artery dissection Vertebral artery dissection Familial aortic dissection Vascular malformation Arteriovenous fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Vascular nevus Cherry hemangioma Halo nevus Spider angioma Veins Inflammation Phlebitis Venous thrombosis / Thrombophlebitis primarily lower limb Deep vein thrombosis abdomen Hepatic veno-occlusive disease Budd–Chiari syndrome May–Thurner syndrome Portal vein thrombosis Renal vein thrombosis upper limb / torso Mondor's disease Paget–Schroetter disease head Cerebral venous sinus thrombosis Post-thrombotic syndrome Varicose veins Gastric varices Portacaval anastomosis Caput medusae Esophageal varices Hemorrhoid Varicocele Other Chronic venous insufficiency Chronic cerebrospinal venous insufficiency Superior vena cava syndrome Inferior vena cava syndrome Venous ulcer Arteries or veins Angiopathy Macroangiopathy Microangiopathy Embolism Pulmonary embolism Cholesterol embolism Paradoxical embolism Thrombosis Vasculitis Blood pressure Hypertension Hypertensive heart disease Hypertensive emergency Hypertensive nephropathy Essential hypertension Secondary hypertension Renovascular hypertension Benign hypertension Pulmonary hypertension Systolic hypertension White coat hypertension Hypotension Orthostatic hypotensionEPAS1, MDM2, BAD, BAK1, BAX, CASP3, EIF3E, SIRT2, BBC3, LMNA, MPL, JAK2, ZMPSTE24, TET2, XYLT2, XYLT1, AGXT, ABCC6, VEGFA, IL6, TNF, PADI4, CRP, DHX40, GSTK1, TIMP2, BCAR1, AGXT2, CACNA1G-AS1, SLCO6A1, NLRP1, RBM45, UGT1A1, ANGPTL6, FURIN, SERPINE1, ACR, NHS, FGF2, ALDH7A1, COL2A1, COX8A, VCAN, ACE, ENG, ESR1, F5, F8, FGF13, NFE2L2, GABPA, HIF1A, HLA-A, HLA-DRB1, HMGB1, KLRB1, ADRB2, LPA, MTHFR, C20orf181
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Dermatofibroma
Wikipedia
External links [ edit ] Classification D ICD - 10 : D23 ( ILDS D23.L62) ICD - 9-CM : 216.9 ICD-O : M8830/0 MeSH : D018219 DiseasesDB : 29384 External resources eMedicine : derm/96 Patient UK : Dermatofibroma v t e Diseases of the skin and appendages by morphology Growths Epidermal Wart Callus Seborrheic keratosis Acrochordon Molluscum contagiosum Actinic keratosis Squamous-cell carcinoma Basal-cell carcinoma Merkel-cell carcinoma Nevus sebaceous Trichoepithelioma Pigmented Freckles Lentigo Melasma Nevus Melanoma Dermal and subcutaneous Epidermal inclusion cyst Hemangioma Dermatofibroma (benign fibrous histiocytoma) Keloid Lipoma Neurofibroma Xanthoma Kaposi's sarcoma Infantile digital fibromatosis Granular cell tumor Leiomyoma Lymphangioma circumscriptum Myxoid cyst Rashes With epidermal involvement Eczematous Contact dermatitis Atopic dermatitis Seborrheic dermatitis Stasis dermatitis Lichen simplex chronicus Darier's disease Glucagonoma syndrome Langerhans cell histiocytosis Lichen sclerosus Pemphigus foliaceus Wiskott–Aldrich syndrome Zinc deficiency Scaling Psoriasis Tinea ( Corporis Cruris Pedis Manuum Faciei ) Pityriasis rosea Secondary syphilis Mycosis fungoides Systemic lupus erythematosus Pityriasis rubra pilaris Parapsoriasis Ichthyosis Blistering Herpes simplex Herpes zoster Varicella Bullous impetigo Acute contact dermatitis Pemphigus vulgaris Bullous pemphigoid Dermatitis herpetiformis Porphyria cutanea tarda Epidermolysis bullosa simplex Papular Scabies Insect bite reactions Lichen planus Miliaria Keratosis pilaris Lichen spinulosus Transient acantholytic dermatosis Lichen nitidus Pityriasis lichenoides et varioliformis acuta Pustular Acne vulgaris Acne rosacea Folliculitis Impetigo Candidiasis Gonococcemia Dermatophyte Coccidioidomycosis Subcorneal pustular dermatosis Hypopigmented Tinea versicolor Vitiligo Pityriasis alba Postinflammatory hyperpigmentation Tuberous sclerosis Idiopathic guttate hypomelanosis Leprosy Hypopigmented mycosis fungoides Without epidermal involvement Red Blanchable Erythema Generalized Drug eruptions Viral exanthems Toxic erythema Systemic lupus erythematosus Localized Cellulitis Abscess Boil Erythema nodosum Carcinoid syndrome Fixed drug eruption Specialized Urticaria Erythema ( Multiforme Migrans Gyratum repens Annulare centrifugum Ab igne ) Nonblanchable Purpura Macular Thrombocytopenic purpura Actinic/solar purpura Papular Disseminated intravascular coagulation Vasculitis Indurated Scleroderma / morphea Granuloma annulare Lichen sclerosis et atrophicus Necrobiosis lipoidica Miscellaneous disorders Ulcers Hair Telogen effluvium Androgenic alopecia Alopecia areata Systemic lupus erythematosus Tinea capitis Loose anagen syndrome Lichen planopilaris Folliculitis decalvans Acne keloidalis nuchae Nail Onychomycosis Psoriasis Paronychia Ingrown nail Mucous membrane Aphthous stomatitis Oral candidiasis Lichen planus Leukoplakia Pemphigus vulgaris Mucous membrane pemphigoid Cicatricial pemphigoid Herpesvirus Coxsackievirus Syphilis Systemic histoplasmosis Squamous-cell carcinoma v t e Connective / soft tissue tumors and sarcomas Not otherwise specified Soft-tissue sarcoma Desmoplastic small-round-cell tumor Connective tissue neoplasm Fibromatous Fibroma / fibrosarcoma : Dermatofibrosarcoma protuberans Desmoplastic fibroma Fibroma / fibromatosis : Aggressive infantile fibromatosis Aponeurotic fibroma Collagenous fibroma Diffuse infantile fibromatosis Familial myxovascular fibromas Fibroma of tendon sheath Fibromatosis colli Infantile digital fibromatosis Juvenile hyaline fibromatosis Plantar fibromatosis Pleomorphic fibroma Oral submucous fibrosis Histiocytoma / histiocytic sarcoma : Benign fibrous histiocytoma Malignant fibrous histiocytoma Atypical fibroxanthoma Solitary fibrous tumor Myxomatous Myxoma / myxosarcoma Cutaneous myxoma Superficial acral fibromyxoma Angiomyxoma Ossifying fibromyxoid tumour Fibroepithelial Brenner tumour Fibroadenoma Phyllodes tumor Synovial -like Synovial sarcoma Clear-cell sarcoma Lipomatous Lipoma / liposarcoma Myelolipoma Myxoid liposarcoma PEComa Angiomyolipoma Chondroid lipoma Intradermal spindle cell lipoma Pleomorphic lipoma Lipoblastomatosis Spindle cell lipoma Hibernoma Myomatous general: Myoma / myosarcoma smooth muscle : Leiomyoma / leiomyosarcoma skeletal muscle : Rhabdomyoma / rhabdomyosarcoma : Embryonal rhabdomyosarcoma Sarcoma botryoides Alveolar rhabdomyosarcoma Leiomyoma Angioleiomyoma Angiolipoleiomyoma Genital leiomyoma Leiomyosarcoma Multiple cutaneous and uterine leiomyomatosis syndrome Multiple cutaneous leiomyoma Neural fibrolipoma Solitary cutaneous leiomyoma STUMP Complex mixed and stromal Adenomyoma Pleomorphic adenoma Mixed Müllerian tumor Mesoblastic nephroma Wilms' tumor Malignant rhabdoid tumour Clear-cell sarcoma of the kidney Hepatoblastoma Pancreatoblastoma Carcinosarcoma Mesothelial Mesothelioma Adenomatoid tumor v t e Skin cancer of the dermis Dermis Benign fibrous histiocytoma / dermatofibrosarcoma protuberans Dermatofibrosarcoma protuberans Subcutaneous tumors Connective and vascular see Template:Soft tissue tumors and sarcomas , Template:Vascular tumors , Template:Myeloid malignancy (for mastocytosis ) Other urogenital: Hirsuties coronae glandis neuro: Solitary neurofibroma Cutaneous meningioma Ganglioneuroma Schwannoma Palisaded encapsulated neuroma Infantile neuroblastoma Neuroma cutis bone/cartilage: Chordoma Extraskeletal chondroma nevus: Nevus anemicus Nevus flammeus Nevus flammeus nuchae Nevus lipomatosus superficialis Nevus oligemicus Connective tissue nevus Midline nevus flammeus Porokeratotic eccrine ostial and dermal duct nevus histiocytoma : Pleomorphic undifferentiated sarcoma Plexiform fibrohistiocytic tumor Progressive nodular histiocytoma Teratoma Adenoma sebaceum Metastatic carcinoma Giant-cell tumor of the tendon sheath Glomus tumor Granular cell tumor Carcinoid Desmoid tumor Neurothekeoma Angiokeratoma Zosteriform metastasis Keratinizing metaplasia Epithelioid sarcoma
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Inverted Nipple
Wikipedia
Contents 1 Causes 2 Grading system 3 Pregnancy and breastfeeding 4 Piercing 5 Other corrective strategies 6 References 7 External links Causes [ edit ] The most common causes of nipple inversion include: Born with condition Trauma which can be caused by conditions such as fat necrosis , scars, or a result of surgery Breast sagging, drooping or ptosis Breast cancer Breast carcinoma Paget's disease Inflammatory breast cancer Breast infections or inflammations Mammary duct ectasia Breast abscess Mastitis Genetic variant of nipple shape, such as: Weaver syndrome Congenital disorder of glycosylation type 1A and 1 L Kennerknecht-Sorgo-Oberhoffer syndrome Gynecomastia Recurrent infections Tuberculosis Around 10–20% of all women are born with this condition. [1] Most common nipple variations that women are born with are caused by short ducts or a wide areola muscle sphincter . ... External links [ edit ] Classification D ICD - 10 : N64.5 , O92.0 ICD - 9-CM : 611.8 Inflammatory Breast Cancer Inversion of Nipple v t e Breast disease Inflammation Mastitis Nonpuerperal mastitis Subareolar abscess Granulomatous mastitis Physiological changes and conditions Benign mammary dysplasia Duct ectasia of breast Chronic cystic mastitis Mammoplasia Gynecomastia Adipomastia (lipomastia, pseudogynecomastia) Breast hypertrophy Breast atrophy Micromastia Amastia Anisomastia Breast engorgement Nipple Nipple discharge Galactorrhea Inverted nipple Cracked nipples Nipple pigmentation Masses Galactocele Breast cyst Breast hematoma Breast lump Pseudoangiomatous stromal hyperplasia Other Pain Tension Ptosis Fat necrosis Amazia v t e Pathology of pregnancy , childbirth and the puerperium Pregnancy Pregnancy with abortive outcome Abortion Ectopic pregnancy Abdominal Cervical Interstitial Ovarian Heterotopic Embryo loss Fetal resorption Molar pregnancy Miscarriage Stillbirth Oedema , proteinuria and hypertensive disorders Gestational hypertension Pre-eclampsia HELLP syndrome Eclampsia Other, predominantly related to pregnancy Digestive system Acute fatty liver of pregnancy Gestational diabetes Hepatitis E Hyperemesis gravidarum Intrahepatic cholestasis of pregnancy Integumentary system / dermatoses of pregnancy Gestational pemphigoid Impetigo herpetiformis Intrahepatic cholestasis of pregnancy Linea nigra Prurigo gestationis Pruritic folliculitis of pregnancy Pruritic urticarial papules and plaques of pregnancy (PUPPP) Striae gravidarum Nervous system Chorea gravidarum Blood Gestational thrombocytopenia Pregnancy-induced hypercoagulability Maternal care related to the fetus and amniotic cavity amniotic fluid Oligohydramnios Polyhydramnios Braxton Hicks contractions chorion / amnion Amniotic band syndrome Chorioamnionitis Chorionic hematoma Monoamniotic twins Premature rupture of membranes Obstetrical bleeding Antepartum placenta Circumvallate placenta Monochorionic twins Placenta accreta Placenta praevia Placental abruption Twin-to-twin transfusion syndrome Labor Amniotic fluid embolism Cephalopelvic disproportion Dystocia Shoulder dystocia Fetal distress Locked twins Nuchal cord Obstetrical bleeding Postpartum Pain management during childbirth placenta Placenta accreta Preterm birth Postmature birth Umbilical cord prolapse Uterine inversion Uterine rupture Vasa praevia Puerperal Breastfeeding difficulties Low milk supply Cracked nipples Breast engorgement Childbirth-related posttraumatic stress disorder Diastasis symphysis pubis Postpartum bleeding Peripartum cardiomyopathy Postpartum depression Postpartum psychosis Postpartum thyroiditis Puerperal fever Puerperal mastitis Other Concomitant conditions Diabetes mellitus Systemic lupus erythematosus Thyroid disorders Maternal death Sexual activity during pregnancy Category
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Uterine Rupture
Wikipedia
In 2006, an extremely rare case of uterine rupture in a first pregnancy with no risk factors was reported. [8] Uterine rupture during pregnancy without a prior cesarean section is one of the major diagnostic criterion for vascular Ehlers-Danlos syndrome (vEDS). [9] Mechanism [ edit ] In an incomplete rupture the peritoneum is still intact. ... S2CID 8021433 . ^ Byers, Peter H. (2019). Vascular Ehlers-Danlos Syndrome . University of Washington, Seattle. External links [ edit ] Classification D ICD - 10 : O71.0 - O71.1 ICD - 9-CM : 665.1 MeSH : D014597 DiseasesDB : 13642 External resources eMedicine : med/3746 v t e Pathology of pregnancy , childbirth and the puerperium Pregnancy Pregnancy with abortive outcome Abortion Ectopic pregnancy Abdominal Cervical Interstitial Ovarian Heterotopic Embryo loss Fetal resorption Molar pregnancy Miscarriage Stillbirth Oedema , proteinuria and hypertensive disorders Gestational hypertension Pre-eclampsia HELLP syndrome Eclampsia Other, predominantly related to pregnancy Digestive system Acute fatty liver of pregnancy Gestational diabetes Hepatitis E Hyperemesis gravidarum Intrahepatic cholestasis of pregnancy Integumentary system / dermatoses of pregnancy Gestational pemphigoid Impetigo herpetiformis Intrahepatic cholestasis of pregnancy Linea nigra Prurigo gestationis Pruritic folliculitis of pregnancy Pruritic urticarial papules and plaques of pregnancy (PUPPP) Striae gravidarum Nervous system Chorea gravidarum Blood Gestational thrombocytopenia Pregnancy-induced hypercoagulability Maternal care related to the fetus and amniotic cavity amniotic fluid Oligohydramnios Polyhydramnios Braxton Hicks contractions chorion / amnion Amniotic band syndrome Chorioamnionitis Chorionic hematoma Monoamniotic twins Premature rupture of membranes Obstetrical bleeding Antepartum placenta Circumvallate placenta Monochorionic twins Placenta accreta Placenta praevia Placental abruption Twin-to-twin transfusion syndrome Labor Amniotic fluid embolism Cephalopelvic disproportion Dystocia Shoulder dystocia Fetal distress Locked twins Nuchal cord Obstetrical bleeding Postpartum Pain management during childbirth placenta Placenta accreta Preterm birth Postmature birth Umbilical cord prolapse Uterine inversion Uterine rupture Vasa praevia Puerperal Breastfeeding difficulties Low milk supply Cracked nipples Breast engorgement Childbirth-related posttraumatic stress disorder Diastasis symphysis pubis Postpartum bleeding Peripartum cardiomyopathy Postpartum depression Postpartum psychosis Postpartum thyroiditis Puerperal fever Puerperal mastitis Other Concomitant conditions Diabetes mellitus Systemic lupus erythematosus Thyroid disorders Maternal death Sexual activity during pregnancy Category
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Hereditary Coproporphyria
Wikipedia
External links [ edit ] Classification D ICD - 10 : E80.2 ( ILDS E80.222) ICD - 9-CM : 277.1 OMIM : 121300 MeSH : D046349 DiseasesDB : 30591 External resources eMedicine : med/1888 Porphyria at NLM Genetics Home Reference Coproporphyria at NIH 's Office of Rare Diseases MedlinePlus Encyclopedia : Porphyria v t e Heme metabolism disorders Porphyria , hepatic and erythropoietic ( porphyrin ) early mitochondrial: ALAD porphyria Acute intermittent porphyria cytoplasmic: Gunther disease/congenital erythropoietic porphyria Porphyria cutanea tarda / Hepatoerythropoietic porphyria late mitochondrial: Hereditary coproporphyria Harderoporphyria Variegate porphyria Erythropoietic protoporphyria Hereditary hyperbilirubinemia ( bilirubin ) unconjugated: Gilbert's syndrome Crigler–Najjar syndrome Lucey–Driscoll syndrome conjugated: Dubin–Johnson syndrome nd sheet Rotor syndrome
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Obsessive-Compulsive Disorder
Omim
Other Features Leckman et al. (1994) found higher levels of oxytocin (167050) in the lumbar spinal fluid of patients with obsessive-compulsive disorder but no personal or family history of tics, than in normal controls or patients with obsessive-compulsive disorder in the presence of Tourette syndrome. In contrast to previous reports, they found similar concentrations of arginine vasopressin (192340) in the spinal fluid of all 3 groups. ... Although it has been suggested that OCD represents an alternative expression of the gene responsible for Tourette syndrome (137580), the disorder in this family appeared to be clinically distinct. ... Zhang et al. (2002) performed a genomewide scan of hoarding in 77 sib pairs in which both sibs also had Tourette syndrome. Twenty-six pairs were concordant for hoarding, 28 were discordant for hoarding, and 23 with concordant for being unaffected with hoarding. Treating the hoarding as either a dichotomous or a quantitative trait, they found evidence of linkage to chromosome 4q34-q35 in a region where a Tourette syndrome locus had previously been mapped. ... Of 7 family members with the mutation, 6 had OCD and 1 had obsessive-compulsive personality disorder; several of them also met diagnostic criteria for other disorders, including Asperger syndrome (see 608638), social phobia, anorexia nervosa (see 606788), tic disorder, and alcohol (103780) and other substance abuse/dependence.SLC6A4, HTR2A, HOXB8, SLITRK5, CCKBR, HTR1D, BDNF, ADCK1, LINC02395, SLC1A1, TAFA2, NECTIN1, COMT, CARMIL1, GPR135, POU1F1, MAOA, DLGAP3, TNF, DRD4, HTR1B, TPH2, SGCE, GRIN2B, SLITRK1, OXTR, SLC6A3, OLIG2, HTR2C, DRD2, MCF2L, LRP2, HTR3A, DRD3, LOC110806262, GRIK2, CDH2, OPN1SW, NTRK3, IL6, KRT7, ABO, MOG, ACACA, PBX1, TAL1, TYMS, HTT, ARFGEF1, TPSG1, PYCARD, SCLY, EBPL, BMS1, STIN2-VNTR, ELK3, GRM5, CYP2C19, GRN, CYP2D6, TSPO, GAD2, DLG4, AKAP13, GOLGA8A, KDM4C, PRDX5, CYP19A1, ARFGEF2, CNTNAP2, DNM3, DNASE1L3, DRD1, COX8A, HCN4, TOR1A, SETD1A, NOS1AP, PPIG, PDLIM7, DLGAP1, HTR3B, EFNA5, DGKD, TRRAP, UCP2, CUX1, GTS, CHPT1, CNR1, ACTB, ACAN, NPS, MIR485, BDNF-AS, PHOBS, NPSR1, AQP6, HTR3E, C9orf72, HTR3D, SPRED2, ARID2, HTR3C, OR2AG1, RBM45, OLIG1, CACNA1C, BTBD9, DISP1, PPP1R9B, CCT6A, DHDDS, CDH9, TXN, CLA3, THAS, EPHB2, IL17A, NFKBIL1, MTHFR, GABRG2, MEIS2, MECP2, MAP6, LTBP3, GAPDH, LMX1A, LCT, GATA3, KIF22, CXCL8, HLA-DRB1, GCH1, IL1B, IL1A, IGKC, IGF1, IFNG, GDNF, GJB2, HTR2B, GRIA3, GRIK3, HTR1A, NOS1, GABBR1, NTF3, NTRK2, ERCC2, SRM, SRI, SPARC, SLC22A3, SLC18A1, ESR1, ESR2, SLC1A3, SLC1A2, FCGR3A, CCL2, SCN3A, RYR3, FCGR3B, MAPK1, FGFR3, PGC, PDE4D, FKBP5, P2RX7, FOS, OPRM1, OMD, FRAXE, NPY
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Tetrahydrobiopterin Deficiency
Wikipedia
External links [ edit ] Classification D ICD - 10 : E70.1 ICD - 9-CM : 270.1 MeSH : C538382 External resources eMedicine : ped/2226 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 v t e Metabolic disorders of vitamins , coenzymes, and cofactors B7 Biotin / MCD Biotinidase deficiency Holocarboxylase synthetase deficiency Other B B5 ( Pantothenate kinase-associated neurodegeneration ) B12 ( Methylmalonic acidemia ) Other vitamin Familial isolated vitamin E deficiency Nonvitamin cofactor Tetrahydrobiopterin deficiency Molybdenum cofactor deficiency
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Atopic Dermatitis
Medlineplus
Some such disorders are Netherton syndrome; immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome; and severe dermatitis, multiple allergies, metabolic wasting (SAM) syndrome. ... They can affect gene activity and regulate the production of proteins, which may influence the development of allergies in susceptible individuals. Syndromes with atopic dermatitis as one of several features are caused by mutations in other genes.
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Herpetic Whitlow
Wikipedia
Retrieved 2014-05-12 . 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