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Lymphocyte-Variant Hypereosinophilia
Wikipedia
"Recent advances in pathogenesis and management of hypereosinophilic syndromes". Allergy . 59 (7): 673–89. doi : 10.1111/j.1398-9995.2004.00465.x . ... "The lymphoid variant of hypereosinophilic syndrome: study of 21 patients with CD3-CD4+ aberrant T-cell phenotype" . ... "Interleukin-5 is the predominant eosinophilopoietin produced by cloned T lymphocytes in hypereosinophilic syndrome". Experimental Hematology . 21 (2): 358–65. ... "Management of Hypereosinophilic Syndromes". Immunology and Allergy Clinics of North America . 35 (3): 561–75. doi : 10.1016/j.iac.2015.05.006 . ... Clonal analysis in an idiopathic hypereosinophilic syndrome". Journal of Immunology . 139 (11): 3753–8.
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Episcleritis
Wikipedia
An identifiable cause is discovered in about one third of cases. [6] Several diseases are associated with episcleritis, including systemic vasculitis ( polyarteritis nodosa , granulomatosis with polyangiitis , Behçet's disease ), connective tissue diseases ( rheumatoid arthritis , relapsing polychondritis , systemic lupus erythematosus ), [7] psoriatic arthritis , ankylosing spondylitis , Cogan syndrome , rosacea , gout , [4] atopy , [6] Crohn's disease , and ulcerative colitis . [8] [5] 59 percent of patients with relapsing polychondritis have either episcleritis or scleritis. [9] Rarely, episcleritis may be caused by scleritis . [10] Very rarely, episcleritis is associated with infections, including Lyme disease , tuberculosis , syphilis , and herpes zoster . [5] The redness in the eye associated with episcleritis is due to engorgement of the large episcleral blood vessels, which run in a radial direction from the limbus . [4] Typically, there is no uveitis, or thickening of the sclera. ... External links [ edit ] Classification D ICD - 10 : H15.1 ICD - 9-CM : 379.0 MeSH : D015423 DiseasesDB : 4375 External resources MedlinePlus : 001019 v t e Diseases of the human eye Adnexa Eyelid Inflammation Stye Chalazion Blepharitis Entropion Ectropion Lagophthalmos Blepharochalasis Ptosis Blepharophimosis Xanthelasma Ankyloblepharon Eyelash Trichiasis Madarosis Lacrimal apparatus Dacryoadenitis Epiphora Dacryocystitis Xerophthalmia Orbit Exophthalmos Enophthalmos Orbital cellulitis Orbital lymphoma Periorbital cellulitis Conjunctiva Conjunctivitis allergic Pterygium Pseudopterygium Pinguecula Subconjunctival hemorrhage Globe Fibrous tunic Sclera Scleritis Episcleritis Cornea Keratitis herpetic acanthamoebic fungal Exposure Photokeratitis Corneal ulcer Thygeson's superficial punctate keratopathy Corneal dystrophy Fuchs' Meesmann Corneal ectasia Keratoconus Pellucid marginal degeneration Keratoglobus Terrien's marginal degeneration Post-LASIK ectasia Keratoconjunctivitis sicca Corneal opacity Corneal neovascularization Kayser–Fleischer ring Haab's striae Arcus senilis Band keratopathy Vascular tunic Iris Ciliary body Uveitis Intermediate uveitis Hyphema Rubeosis iridis Persistent pupillary membrane Iridodialysis Synechia Choroid Choroideremia Choroiditis Chorioretinitis Lens Cataract Congenital cataract Childhood cataract Aphakia Ectopia lentis Retina Retinitis Chorioretinitis Cytomegalovirus retinitis Retinal detachment Retinoschisis Ocular ischemic syndrome / Central retinal vein occlusion Central retinal artery occlusion Branch retinal artery occlusion Retinopathy diabetic hypertensive Purtscher's of prematurity Bietti's crystalline dystrophy Coats' disease Sickle cell Macular degeneration Retinitis pigmentosa Retinal haemorrhage Central serous retinopathy Macular edema Epiretinal membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary juvenile glaucoma Floater Leber's hereditary optic neuropathy Red eye Globe rupture Keratomycosis Phthisis bulbi Persistent fetal vasculature / Persistent hyperplastic primary vitreous Persistent tunica vasculosa lentis Familial exudative vitreoretinopathy Pathways Optic nerve Optic disc Optic neuritis optic papillitis Papilledema Foster Kennedy syndrome Optic atrophy Optic disc drusen Optic neuropathy Ischemic anterior (AION) posterior (PION) Kjer's Leber's hereditary Toxic and nutritional Strabismus Extraocular muscles Binocular vision Accommodation Paralytic strabismus Ophthalmoparesis Chronic progressive external ophthalmoplegia Kearns–Sayre syndrome palsies Oculomotor (III) Fourth-nerve (IV) Sixth-nerve (VI) Other strabismus Esotropia / Exotropia Hypertropia Heterophoria Esophoria Exophoria Cyclotropia Brown's syndrome Duane syndrome Other binocular Conjugate gaze palsy Convergence insufficiency Internuclear ophthalmoplegia One and a half syndrome Refraction Refractive error Hyperopia Myopia Astigmatism Anisometropia / Aniseikonia Presbyopia Vision disorders Blindness Amblyopia Leber's congenital amaurosis Diplopia Scotoma Color blindness Achromatopsia Dichromacy Monochromacy Nyctalopia Oguchi disease Blindness / Vision loss / Visual impairment Anopsia Hemianopsia binasal bitemporal homonymous Quadrantanopia subjective Asthenopia Hemeralopia Photophobia Scintillating scotoma Pupil Anisocoria Argyll Robertson pupil Marcus Gunn pupil Adie syndrome Miosis Mydriasis Cycloplegia Parinaud's syndrome Other Nystagmus Childhood blindness Infections Trachoma Onchocerciasis
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Farmer's Lung
Wikipedia
External links [ edit ] Classification D ICD - 10 : J67.0 ICD - 9-CM : 495.0 MeSH : D005203 DiseasesDB : 29636 External resources eMedicine : med/771 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 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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Heart Block
Wikipedia
External links [ edit ] Classification D ICD - 10 : I44 - I45 ICD - 9-CM : 426.9 MeSH : D006327 DiseasesDB : 10477 v t e Cardiovascular disease (heart) Ischaemic Coronary disease Coronary artery disease (CAD) Coronary artery aneurysm Spontaneous coronary artery dissection (SCAD) Coronary thrombosis Coronary vasospasm Myocardial bridge Active ischemia Angina pectoris Prinzmetal's angina Stable angina Acute coronary syndrome Myocardial infarction Unstable angina Sequelae hours Hibernating myocardium Myocardial stunning days Myocardial rupture weeks Aneurysm of heart / Ventricular aneurysm Dressler syndrome Layers Pericardium Pericarditis Acute Chronic / Constrictive Pericardial effusion Cardiac tamponade Hemopericardium Myocardium Myocarditis Chagas disease Cardiomyopathy Dilated Alcoholic Hypertrophic Tachycardia-induced Restrictive Loeffler endocarditis Cardiac amyloidosis Endocardial fibroelastosis Arrhythmogenic right ventricular dysplasia Endocardium / valves Endocarditis infective endocarditis Subacute bacterial endocarditis non-infective endocarditis Libman–Sacks endocarditis Nonbacterial thrombotic endocarditis Valves mitral regurgitation prolapse stenosis aortic stenosis insufficiency tricuspid stenosis insufficiency pulmonary stenosis insufficiency Conduction / arrhythmia Bradycardia Sinus bradycardia Sick sinus syndrome Heart block : Sinoatrial AV 1° 2° 3° Intraventricular Bundle branch block Right Left Left anterior fascicle Left posterior fascicle Bifascicular Trifascicular Adams–Stokes syndrome Tachycardia ( paroxysmal and sinus ) Supraventricular Atrial Multifocal Junctional AV nodal reentrant Junctional ectopic Ventricular Accelerated idioventricular rhythm Catecholaminergic polymorphic Torsades de pointes Premature contraction Atrial Junctional Ventricular Pre-excitation syndrome Lown–Ganong–Levine Wolff–Parkinson–White Flutter / fibrillation Atrial flutter Ventricular flutter Atrial fibrillation Familial Ventricular fibrillation Pacemaker Ectopic pacemaker / Ectopic beat Multifocal atrial tachycardia Pacemaker syndrome Parasystole Wandering atrial pacemaker Long QT syndrome Andersen–Tawil Jervell and Lange-Nielsen Romano–Ward Cardiac arrest Sudden cardiac death Asystole Pulseless electrical activity Sinoatrial arrest Other / ungrouped hexaxial reference system Right axis deviation Left axis deviation QT Short QT syndrome T T wave alternans ST Osborn wave ST elevation ST depression Strain pattern Cardiomegaly Ventricular hypertrophy Left Right / Cor pulmonale Atrial enlargement Left Right Athletic heart syndrome Other Cardiac fibrosis Heart failure Diastolic heart failure Cardiac asthma Rheumatic fever
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Poikiloderma Vasculare Atrophicans
Wikipedia
The condition may also be caused by, associated with or accompany any of the following conditions or disorders: other skin lymphomas, dermatomyositis , lupus erythematosus , Rothmund–Thomson syndrome , Kindler syndrome , dyskeratosis congenita , and chronic radiodermatitis . [4] Rare causes include arsenic ingestion, and the condition can also be idiopathic . [1] [3] [5] PVA may be considered a rare variant of cutaneous T-cell lymphoma , a non-Hodgkin's form of lymphoma affecting the skin. [7] It may also be included among a number of similar conditions that are considered as precursors to mycosis fungoides . PVA is believed to be a syndrome closely associated with large-plaque parapsoriasis and its cohort retiform parapsoriasis ; including PVA, all three conditions fit within an updated view of the once ambiguous classification scheme known as parapsoriasis . [5] Contents 1 Presentation 2 Cause 3 Diagnosis 3.1 Classification 4 Management 5 See also 6 References 7 External links Presentation [ edit ] The layers of the epidermis (left). ... Among them, xeroderma pigmentosum and Rothmund–Thomson syndrome (poikiloderma congenita) are thought to be the most prominent. [5] Ingestion of substances containing arsenic , such as arsphenamine , has also been suggested as a least common cause. [5] PVA can also be idiopathic (of unknown cause), as seen in a small number of cases. [5] Diagnosis [ edit ] Classification [ edit ] Poikiloderma vasculare atrophicans, or PVA, indicates that extra or altered skin pigmentation (" poikiloderma ") [10] is occurring, associated with heightened visibity of capillaries (" vasculare ", referring to telangiectasia) under the skin, related to thinning and wasting away (" atrophicans ") of the skin and its tissue . ... PVA fits within this updated view of parapsoriasis as a syndrome often associated with large plaque parapsoriasis and, or including its variant form, retiform parapsoriasis. [5] Additionally, it may be considered a precursor or variant of the lymphomatous skin disorder mycosis fungoides, which is also associated with large plaque parapsoriasis. [5] Large plaque parapsoriasis consists of inflamed, oddly discolored (such as yellow or blue), web-patterned and scaling plaques on the skin, 10 cm (3.9 in) or larger in diameter. [5] When the condition of the skin encompassed by these plaques worsens and becomes atrophic, it is typically considered retiform parapsoriasis. [5] PVA can occur in either the large plaque or retiform stage, but it can only be considered PVA when its three constituents (poikiloderma, telangiectasia, atrophy) are present. [5] PVA is therefore considered an independent syndrome identified by its constituents, wherever it occurs. [5] In modern consideration and usage, the solitary term "poikiloderma" has also come to represent all three elements of PVA. [5] When skin diseases and disorders or skin conditions described as dermatoses contain the term poikiloderma in their assessment or diagnosis (such as with Bloom syndrome ), this can sometimes be an erroneous usage of the term. [5] Discretion has been advised. [5] Usage of the entire term "poikiloderma vasculare atrophicans" may also be reserved to indicate it as the primary condition affecting the skin in cases where the disorder associated with it is secondary. [5] Management [ edit ] This section is empty. ... External links [ edit ] Classification D ICD - 10 : L94.5 ICD - 9-CM : 696.2 DiseasesDB : 10208 v t e Cutaneous keratosis, ulcer, atrophy, and necrobiosis Epidermal thickening keratoderma : Keratoderma climactericum Paraneoplastic keratoderma Acrokeratosis paraneoplastica of Bazex Aquagenic keratoderma Drug-induced keratoderma psoriasis Keratoderma blennorrhagicum keratosis : Seborrheic keratosis Clonal seborrheic keratosis Common seborrheic keratosis Irritated seborrheic keratosis Seborrheic keratosis with squamous atypia Reticulated seborrheic keratosis Dermatosis papulosa nigra Keratosis punctata of the palmar creases other hyperkeratosis : Acanthosis nigricans Confluent and reticulated papillomatosis Callus Ichthyosis acquisita Arsenical keratosis Chronic scar keratosis Hyperkeratosis lenticularis perstans Hydrocarbon keratosis Hyperkeratosis of the nipple and areola Inverted follicular keratosis Lichenoid keratosis Multiple minute digitate hyperkeratosis PUVA keratosis Reactional keratosis Stucco keratosis Thermal keratosis Viral keratosis Warty dyskeratoma Waxy keratosis of childhood other hypertrophy: Keloid Hypertrophic scar Cutis verticis gyrata Necrobiosis / granuloma Necrobiotic/palisading Granuloma annulare Perforating Generalized Subcutaneous Granuloma annulare in HIV disease Localized granuloma annulare Patch-type granuloma annulare Necrobiosis lipoidica Annular elastolytic giant-cell granuloma Granuloma multiforme Necrobiotic xanthogranuloma Palisaded neutrophilic and granulomatous dermatitis Rheumatoid nodulosis Interstitial granulomatous dermatitis / Interstitial granulomatous drug reaction Foreign body granuloma Beryllium granuloma Mercury granuloma Silica granuloma Silicone granuloma Zirconium granuloma Soot tattoo Tattoo Carbon stain Other/ungrouped eosinophilic dermatosis Granuloma faciale Dermis / localized CTD Cutaneous lupus erythematosus chronic: Discoid Panniculitis subacute : Neonatal ungrouped: Chilblain Lupus erythematosus–lichen planus overlap syndrome Tumid Verrucous Rowell's syndrome Scleroderma / Morphea Localized scleroderma Localized morphea Morphea–lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma Atrophic / atrophoderma Lichen sclerosus Anetoderma Schweninger–Buzzi anetoderma Jadassohn–Pellizzari anetoderma Atrophoderma of Pasini and Pierini Acrodermatitis chronica atrophicans Semicircular lipoatrophy Follicular atrophoderma Linear atrophoderma of Moulin Perforating Kyrle disease Reactive perforating collagenosis Elastosis perforans serpiginosa Perforating folliculitis Acquired perforating dermatosis Skin ulcer Pyoderma gangrenosum Other Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum / Pseudo-ainhum
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Bad Trip
Wikipedia
Psychedelics in the Psychiatric ER - Julie Holland, M.D. lecture in the Psychedelic Science in the 21st Century conference in 2010. v t e Psychoactive substance-related disorder General SID Substance intoxication / Drug overdose Substance-induced psychosis Withdrawal : Craving Neonatal withdrawal Post-acute-withdrawal syndrome (PAWS) SUD Substance abuse / Substance-related disorders Physical dependence / Psychological dependence / Substance dependence Combined substance use SUD Polysubstance dependence SID Combined drug intoxication (CDI) Alcohol SID Cardiovascular diseases Alcoholic cardiomyopathy Alcohol flush reaction (AFR) Gastrointestinal diseases Alcoholic liver disease (ALD): Alcoholic hepatitis Auto-brewery syndrome (ABS) Endocrine diseases Alcoholic ketoacidosis (AKA) Nervous system diseases Alcohol-related dementia (ARD) Alcohol intoxication Hangover Neurological disorders Alcoholic hallucinosis Alcoholic polyneuropathy Alcohol-related brain damage Alcohol withdrawal syndrome (AWS): Alcoholic hallucinosis Delirium tremens (DTs) Fetal alcohol spectrum disorder (FASD) Fetal alcohol syndrome (FAS) Korsakoff syndrome Positional alcohol nystagmus (PAN) Wernicke–Korsakoff syndrome (WKS, Korsakoff psychosis) Wernicke encephalopathy (WE) Respiratory tract diseases Alcohol-induced respiratory reactions Alcoholic lung disease SUD Alcoholism (alcohol use disorder (AUD)) Binge drinking Caffeine SID Caffeine-induced anxiety disorder Caffeine-induced sleep disorder Caffeinism SUD Caffeine dependence Cannabis SID Cannabis arteritis Cannabinoid hyperemesis syndrome (CHS) SUD Amotivational syndrome Cannabis use disorder (CUD) Synthetic cannabinoid use disorder Cocaine SID Cocaine intoxication Prenatal cocaine exposure (PCE) SUD Cocaine dependence Hallucinogen SID Acute intoxication from hallucinogens (bad trip) Hallucinogen persisting perception disorder (HPPD) Nicotine SID Nicotine poisoning Nicotine withdrawal SUD Nicotine dependence Opioids SID Opioid overdose SUD Opioid use disorder (OUD) Sedative / hypnotic SID Kindling (sedative–hypnotic withdrawal) benzodiazepine : SID Benzodiazepine overdose Benzodiazepine withdrawal SUD Benzodiazepine use disorder (BUD) Benzodiazepine dependence barbiturate : SID Barbiturate overdose SUD Barbiturate dependence Stimulants SID Stimulant psychosis amphetamine : SUD Amphetamine dependence Volatile solvent SID Sudden sniffing death syndrome (SSDS) Toluene toxicity SUD Inhalant abuse
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Scintillating Scotoma
Wikipedia
External links [ edit ] Classification D ICD - 10 : H53.1 ICD - 9-CM : 368.12 OMIM : 613656 MeSH : D012607 External resources eMedicine : neuro/480 v t e Diseases of the human eye Adnexa Eyelid Inflammation Stye Chalazion Blepharitis Entropion Ectropion Lagophthalmos Blepharochalasis Ptosis Blepharophimosis Xanthelasma Ankyloblepharon Eyelash Trichiasis Madarosis Lacrimal apparatus Dacryoadenitis Epiphora Dacryocystitis Xerophthalmia Orbit Exophthalmos Enophthalmos Orbital cellulitis Orbital lymphoma Periorbital cellulitis Conjunctiva Conjunctivitis allergic Pterygium Pseudopterygium Pinguecula Subconjunctival hemorrhage Globe Fibrous tunic Sclera Scleritis Episcleritis Cornea Keratitis herpetic acanthamoebic fungal Exposure Photokeratitis Corneal ulcer Thygeson's superficial punctate keratopathy Corneal dystrophy Fuchs' Meesmann Corneal ectasia Keratoconus Pellucid marginal degeneration Keratoglobus Terrien's marginal degeneration Post-LASIK ectasia Keratoconjunctivitis sicca Corneal opacity Corneal neovascularization Kayser–Fleischer ring Haab's striae Arcus senilis Band keratopathy Vascular tunic Iris Ciliary body Uveitis Intermediate uveitis Hyphema Rubeosis iridis Persistent pupillary membrane Iridodialysis Synechia Choroid Choroideremia Choroiditis Chorioretinitis Lens Cataract Congenital cataract Childhood cataract Aphakia Ectopia lentis Retina Retinitis Chorioretinitis Cytomegalovirus retinitis Retinal detachment Retinoschisis Ocular ischemic syndrome / Central retinal vein occlusion Central retinal artery occlusion Branch retinal artery occlusion Retinopathy diabetic hypertensive Purtscher's of prematurity Bietti's crystalline dystrophy Coats' disease Sickle cell Macular degeneration Retinitis pigmentosa Retinal haemorrhage Central serous retinopathy Macular edema Epiretinal membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary juvenile glaucoma Floater Leber's hereditary optic neuropathy Red eye Globe rupture Keratomycosis Phthisis bulbi Persistent fetal vasculature / Persistent hyperplastic primary vitreous Persistent tunica vasculosa lentis Familial exudative vitreoretinopathy Pathways Optic nerve Optic disc Optic neuritis optic papillitis Papilledema Foster Kennedy syndrome Optic atrophy Optic disc drusen Optic neuropathy Ischemic anterior (AION) posterior (PION) Kjer's Leber's hereditary Toxic and nutritional Strabismus Extraocular muscles Binocular vision Accommodation Paralytic strabismus Ophthalmoparesis Chronic progressive external ophthalmoplegia Kearns–Sayre syndrome palsies Oculomotor (III) Fourth-nerve (IV) Sixth-nerve (VI) Other strabismus Esotropia / Exotropia Hypertropia Heterophoria Esophoria Exophoria Cyclotropia Brown's syndrome Duane syndrome Other binocular Conjugate gaze palsy Convergence insufficiency Internuclear ophthalmoplegia One and a half syndrome Refraction Refractive error Hyperopia Myopia Astigmatism Anisometropia / Aniseikonia Presbyopia Vision disorders Blindness Amblyopia Leber's congenital amaurosis Diplopia Scotoma Color blindness Achromatopsia Dichromacy Monochromacy Nyctalopia Oguchi disease Blindness / Vision loss / Visual impairment Anopsia Hemianopsia binasal bitemporal homonymous Quadrantanopia subjective Asthenopia Hemeralopia Photophobia Scintillating scotoma Pupil Anisocoria Argyll Robertson pupil Marcus Gunn pupil Adie syndrome Miosis Mydriasis Cycloplegia Parinaud's syndrome Other Nystagmus Childhood blindness Infections Trachoma Onchocerciasis 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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Obsessive–compulsive Spectrum
Wikipedia
Tic disorders [ edit ] Tourette’s syndrome is a neurological disorder characterized by recurrent involuntary movements (motor tics) and involuntary noises (vocal tics). ... Within the population of patients with OCD up to 40% have a history of a tic disorder and 60% of people with Tourette’s syndrome have obsessions and/or compulsions. Plus 30% of people with Tourette’s syndrome have clinically diagnosable OCD. ... PMID 11282689 . ^ Stein DJ, Le Roux L, Bouwer C, Van Heerden B (1998). "Is olfactory reference syndrome an obsessive–compulsive spectrum disorder? ... "Advances in the behavior analytic treatment of trichotillomania and Tourette's Syndrome" . Journal of Early and Intensive Behavior Intervention . 1 (1): 57–64. doi : 10.1037/h0100282 .
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Exotropia
Wikipedia
Strabismus is more common in children with disorders that affect the brain such as cerebral palsy , Down syndrome , hydrocephalus , and brain tumors . ... External links [ edit ] Classification D ICD - 10 : H50.1 , H50.3 ICD - 9-CM : 378.1 MeSH : D005099 DiseasesDB : 33268 eMedicine on congenital exotropia v t e Diseases of the human eye Adnexa Eyelid Inflammation Stye Chalazion Blepharitis Entropion Ectropion Lagophthalmos Blepharochalasis Ptosis Blepharophimosis Xanthelasma Ankyloblepharon Eyelash Trichiasis Madarosis Lacrimal apparatus Dacryoadenitis Epiphora Dacryocystitis Xerophthalmia Orbit Exophthalmos Enophthalmos Orbital cellulitis Orbital lymphoma Periorbital cellulitis Conjunctiva Conjunctivitis allergic Pterygium Pseudopterygium Pinguecula Subconjunctival hemorrhage Globe Fibrous tunic Sclera Scleritis Episcleritis Cornea Keratitis herpetic acanthamoebic fungal Exposure Photokeratitis Corneal ulcer Thygeson's superficial punctate keratopathy Corneal dystrophy Fuchs' Meesmann Corneal ectasia Keratoconus Pellucid marginal degeneration Keratoglobus Terrien's marginal degeneration Post-LASIK ectasia Keratoconjunctivitis sicca Corneal opacity Corneal neovascularization Kayser–Fleischer ring Haab's striae Arcus senilis Band keratopathy Vascular tunic Iris Ciliary body Uveitis Intermediate uveitis Hyphema Rubeosis iridis Persistent pupillary membrane Iridodialysis Synechia Choroid Choroideremia Choroiditis Chorioretinitis Lens Cataract Congenital cataract Childhood cataract Aphakia Ectopia lentis Retina Retinitis Chorioretinitis Cytomegalovirus retinitis Retinal detachment Retinoschisis Ocular ischemic syndrome / Central retinal vein occlusion Central retinal artery occlusion Branch retinal artery occlusion Retinopathy diabetic hypertensive Purtscher's of prematurity Bietti's crystalline dystrophy Coats' disease Sickle cell Macular degeneration Retinitis pigmentosa Retinal haemorrhage Central serous retinopathy Macular edema Epiretinal membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary juvenile glaucoma Floater Leber's hereditary optic neuropathy Red eye Globe rupture Keratomycosis Phthisis bulbi Persistent fetal vasculature / Persistent hyperplastic primary vitreous Persistent tunica vasculosa lentis Familial exudative vitreoretinopathy Pathways Optic nerve Optic disc Optic neuritis optic papillitis Papilledema Foster Kennedy syndrome Optic atrophy Optic disc drusen Optic neuropathy Ischemic anterior (AION) posterior (PION) Kjer's Leber's hereditary Toxic and nutritional Strabismus Extraocular muscles Binocular vision Accommodation Paralytic strabismus Ophthalmoparesis Chronic progressive external ophthalmoplegia Kearns–Sayre syndrome palsies Oculomotor (III) Fourth-nerve (IV) Sixth-nerve (VI) Other strabismus Esotropia / Exotropia Hypertropia Heterophoria Esophoria Exophoria Cyclotropia Brown's syndrome Duane syndrome Other binocular Conjugate gaze palsy Convergence insufficiency Internuclear ophthalmoplegia One and a half syndrome Refraction Refractive error Hyperopia Myopia Astigmatism Anisometropia / Aniseikonia Presbyopia Vision disorders Blindness Amblyopia Leber's congenital amaurosis Diplopia Scotoma Color blindness Achromatopsia Dichromacy Monochromacy Nyctalopia Oguchi disease Blindness / Vision loss / Visual impairment Anopsia Hemianopsia binasal bitemporal homonymous Quadrantanopia subjective Asthenopia Hemeralopia Photophobia Scintillating scotoma Pupil Anisocoria Argyll Robertson pupil Marcus Gunn pupil Adie syndrome Miosis Mydriasis Cycloplegia Parinaud's syndrome Other Nystagmus Childhood blindness Infections Trachoma OnchocerciasisPHOX2A, KIF21A, ACADSB, ADNP, BCOR, CNGB3, P4HTM, PTRH2, SEPSECS, SLC17A5, KDM6B, DNMBP, KDM1A, ATF6, PUF60, SRCAP, TUBB3, WARS2, PHIP, NGLY1, ADD3, ZC4H2, BLOC1S3, EBF3, TANGO2, TMEM67, SLC25A46, LYRM7, UBA5, TMEM231, MRPS34, IRF2BPL, BCORL1, PRR12, GATAD2B, SNX14, FMN2, SCO2, CRIPT, ADGRG1, GNAT2, PIGQ, MYF5, MC1R, SMAD3, HADHA, H3-3A, BPTF, PDE6H, EFNB1, DPAGT1, COL4A1, CNGA3, CDC42, ATRX, PDE6C, OCA2, PEX1, TGFB3, XPA, SLC35A2, UBE3A, TYR, TGFBR2, PRPS1, TGFBR1, TBX1, SOX5, SON, SLC6A8, RPGR, NPHP3-ACAD11, FBN1, FA2H, ERBB4, DES, NES, ATXN3
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Central Retinal Artery Occlusion
Wikipedia
Irreversible damage to neural tissue can occur after approximately 15 minutes of complete blockage to the central retinal artery, but this time may vary between people. [11] Two thirds of people experience 20/400 vision while only one in six will experience 20/40 vision or better. [12] Epidemiology [ edit ] The incidence of CRAO is approximately 1 in 100,000 people in the general population. [13] Risk factors for CRAO include the following: being over 50 years of age, male gender, smoking, hypertension , tranexamic acid, diabetes mellitus , dyslipidemia , angina , valvular disease , transient hemiparesis , cancer, hypercoagulable blood conditions, lupus, or a family history of cerebrovascular or cardiovascular issues. [13] [14] Additional risk factors include endocarditis , atrial myxoma , inflammatory diseases of the blood vessels , and predisposition to forming blood clots . [ citation needed ] See also [ edit ] Amaurosis fugax Ocular ischemic syndrome References [ edit ] ^ a b c d e Varma DD, Cugati S, Lee AW, Chen CS (June 2013). ... External links [ edit ] Classification D External resources eMedicine : article/1223625 v t e Diseases of the human eye Adnexa Eyelid Inflammation Stye Chalazion Blepharitis Entropion Ectropion Lagophthalmos Blepharochalasis Ptosis Blepharophimosis Xanthelasma Ankyloblepharon Eyelash Trichiasis Madarosis Lacrimal apparatus Dacryoadenitis Epiphora Dacryocystitis Xerophthalmia Orbit Exophthalmos Enophthalmos Orbital cellulitis Orbital lymphoma Periorbital cellulitis Conjunctiva Conjunctivitis allergic Pterygium Pseudopterygium Pinguecula Subconjunctival hemorrhage Globe Fibrous tunic Sclera Scleritis Episcleritis Cornea Keratitis herpetic acanthamoebic fungal Exposure Photokeratitis Corneal ulcer Thygeson's superficial punctate keratopathy Corneal dystrophy Fuchs' Meesmann Corneal ectasia Keratoconus Pellucid marginal degeneration Keratoglobus Terrien's marginal degeneration Post-LASIK ectasia Keratoconjunctivitis sicca Corneal opacity Corneal neovascularization Kayser–Fleischer ring Haab's striae Arcus senilis Band keratopathy Vascular tunic Iris Ciliary body Uveitis Intermediate uveitis Hyphema Rubeosis iridis Persistent pupillary membrane Iridodialysis Synechia Choroid Choroideremia Choroiditis Chorioretinitis Lens Cataract Congenital cataract Childhood cataract Aphakia Ectopia lentis Retina Retinitis Chorioretinitis Cytomegalovirus retinitis Retinal detachment Retinoschisis Ocular ischemic syndrome / Central retinal vein occlusion Central retinal artery occlusion Branch retinal artery occlusion Retinopathy diabetic hypertensive Purtscher's of prematurity Bietti's crystalline dystrophy Coats' disease Sickle cell Macular degeneration Retinitis pigmentosa Retinal haemorrhage Central serous retinopathy Macular edema Epiretinal membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary juvenile glaucoma Floater Leber's hereditary optic neuropathy Red eye Globe rupture Keratomycosis Phthisis bulbi Persistent fetal vasculature / Persistent hyperplastic primary vitreous Persistent tunica vasculosa lentis Familial exudative vitreoretinopathy Pathways Optic nerve Optic disc Optic neuritis optic papillitis Papilledema Foster Kennedy syndrome Optic atrophy Optic disc drusen Optic neuropathy Ischemic anterior (AION) posterior (PION) Kjer's Leber's hereditary Toxic and nutritional Strabismus Extraocular muscles Binocular vision Accommodation Paralytic strabismus Ophthalmoparesis Chronic progressive external ophthalmoplegia Kearns–Sayre syndrome palsies Oculomotor (III) Fourth-nerve (IV) Sixth-nerve (VI) Other strabismus Esotropia / Exotropia Hypertropia Heterophoria Esophoria Exophoria Cyclotropia Brown's syndrome Duane syndrome Other binocular Conjugate gaze palsy Convergence insufficiency Internuclear ophthalmoplegia One and a half syndrome Refraction Refractive error Hyperopia Myopia Astigmatism Anisometropia / Aniseikonia Presbyopia Vision disorders Blindness Amblyopia Leber's congenital amaurosis Diplopia Scotoma Color blindness Achromatopsia Dichromacy Monochromacy Nyctalopia Oguchi disease Blindness / Vision loss / Visual impairment Anopsia Hemianopsia binasal bitemporal homonymous Quadrantanopia subjective Asthenopia Hemeralopia Photophobia Scintillating scotoma Pupil Anisocoria Argyll Robertson pupil Marcus Gunn pupil Adie syndrome Miosis Mydriasis Cycloplegia Parinaud's syndrome Other Nystagmus Childhood blindness Infections Trachoma Onchocerciasis
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Patent Ductus Arteriosus
Wikipedia
Condition wherein the ductus arteriosus fails to close after birth Patent ductus arteriosus Other names Persistent ductus arteriosus Diagram of a cross-section through a heart with PDA Specialty Cardiac surgery , paediatrics Symptoms Shortness of breath , failure to thrive , tachycardia , heart murmur Complications Heart failure , Eisenmenger's syndrome , pulmonary hypertension Causes Idiopathic Risk factors Preterm birth , congenital rubella syndrome , chromosomal abnormalities , genetic conditions Diagnostic method Echocardiography , Doppler , X-ray Prevention Screening at birth, high index of suspicion in neonates at risk Treatment NSAIDs , surgery Patent ductus arteriosus ( PDA ) is a medical condition in which the ductus arteriosus fails to close after birth : this allows a portion of oxygenated blood from the left heart to flow back to the lungs by flowing from the aorta, which has a higher pressure, to the pulmonary artery. ... Risk factors [ edit ] Known risk factors include: [ citation needed ] Preterm birth Congenital rubella syndrome Chromosomal abnormalities (e.g., Down syndrome ) Genetic conditions such as Loeys–Dietz syndrome (would also present with other heart defects), Wiedemann–Steiner syndrome , and CHARGE syndrome . ... Prognosis [ edit ] If left untreated, the disease may progress from left-to-right shunt ( acyanotic heart ) to right-to-left shunt ( cyanotic heart ), called Eisenmenger's syndrome . Pulmonary hypertension is a potential long-term outcome, which may require a heart and/or lung transplant . ... Classification D ICD - 10 : Q25.0 ICD - 9-CM : 747.0 OMIM : 607411 MeSH : D004374 DiseasesDB : 9706 External resources MedlinePlus : 001560 eMedicine : emerg/358 Patient UK : Patent ductus arteriosus v t e Congenital vascular defects / Vascular malformation Great arteries / other arteries Aorta Patent ductus arteriosus Coarctation of the aorta Interrupted aortic arch Double aortic arch Right-sided aortic arch Overriding aorta Aneurysm of sinus of Valsalva Vascular ring Pulmonary artery Pulmonary atresia Stenosis of pulmonary artery Subclavian artery Aberrant subclavian artery Umbilical artery Single umbilical artery Great veins Superior / inferior vena cava Congenital stenosis of vena cava Persistent left superior vena cava Pulmonary vein Anomalous pulmonary venous connection ( Total , Partial ) Scimitar syndrome Arteriovenous malformation Cerebral arteriovenous malformation Authority control TA98 : A12.2.01.221TFAP2B, PRDM6, AGTR1, PTGIS, TRAF1, NPPA, KRAS, MYOCD, MYH11, ACTA2, ACTB, TGFBR2, WT1, SMAD4, BRAF, RAC1, TP63, FOXC1, NSD1, SKI, USP9X, TBX5, NKX2-5, GATA4, GJA1, SETD2, BRCA2, MAP3K7, BRCA1, PTPN11, PTEN, G6PC3, LMNA, ZNF148, MKKS, MFAP5, NOTCH2, KAT6A, NOTCH3, XRCC2, PCGF2, ARID1A, SIX6, PCNT, CLIP2, UMPS, NONO, KCNAB2, TRRAP, UBE2A, NFIX, MYLK, DPM1, KYNU, BAZ1B, PIGQ, TRIP11, TRIP4, TBX4, POLR1C, GTF2IRD1, SEC24C, UFD1, PEX1, HIRA, PEX19, RAD51, MASP1, RAD51C, RARB, RBP4, RFC2, RPL5, RPL11, RREB1, SALL1, MAP2K1, SNRPB, SOX2, SSR4, SEMA3E, TALDO1, TBX1, TBX2, PRKG1, TCOF1, PPP1CB, NR2F2, TGFB2, TGFB3, PLAGL1, TGFBR1, TKT, TTC37, TSFM, TMEM94, HYMAI, CRELD1, VPS33A, PORCN, STRA6, PRDM16, FANCM, WDR35, ARID1B, INPP5E, ZEB2, MCTP2, ERMARD, PACS1, PEX26, CHD7, YY1AP1, FANCI, RFWD3, ALG8, FTO, ALG12, THOC6, CTU2, FREM2, KANSL1, JMJD1C, ARX, TMTC3, ESCO2, CEP120, ARL6IP6, B3GLCT, AMER1, SLX4, TRAF7, BRIP1, ADAMTS10, COL18A1, PALB2, FANCL, AGGF1, MKS1, POLR1A, PIGN, KAT6B, LARS2, SIK3, SPECC1L, NEDD4L, PUF60, USP18, ARFGEF2, MAD2L2, APC2, ZMPSTE24, CD96, MYCN, HUWE1, ABCC9, AMMECR1, KCNE5, C2CD3, NCAPG2, PHGDH, BCOR, SAMD9, HYDIN, RAB23, DYNC2LI1, PIGT, DACT1, POLR1D, WDPCP, MRPS16, ASCC1, SLC25A24, UBE2T, CCDC22, AFF4, NPHP3, TBL2, MYH7, SKIV2L, RERE, TMEM258, BMPR1A, GPC4, FBN2, FBN1, ATP5F1D, ARVCF, KCNH1, DHCR7, KCNJ8, DHCR24, DNMT3A, DTNA, DVL3, ECE1, FANCG, FANCF, ARF1, MYRF, FGFR3, LIMK1, FOXF1, GJA8, GPC3, GATA6, GABRD, GLI3, FLNA, GP1BB, FOXC2, CREBBP, COMT, GTF2I, FOXE3, HNRNPK, CHRM3, HPGD, IGBP1, CDC42, FANCB, GJA5, ACSL4, ERCC4, FANCD2, MAT2A, FANCE, FANCC, SMAD3, FANCA, ELN, EP300, LOX, BPTF, MEGF8, ANK1, MAP1B, MUC1, CD274, SPP1, PDX1, TP53, VEGFA, GLI1, ANXA2, AGT, CTNNB1, MBL2, TNFSF10, CDKN2A, MSLN, FOXM1, CYP2C9, CTLA4, CCL2, LGALS1, PDHX, AVSD1, PIK3CG, PIK3CA, MTHFR, FOXA1, COL6A3, HGF, TNF, NOS3, LCN2, MMP7, ERBB2, PTGS2, PDA1, CRP, ENO1, CDK4, PIK3CD, SLC8A1, ARHGAP26, SMARCA4, IL4, SEL1L, PIK3CB, EIF4E, ELAVL1, PLAC8, CXADR, EIF4A2, EIF4G1, PALD1, EIF4A1, CHST15, TRIM29, SGSM3, ACE, SLC45A2, DCC, NTNG1, DCK, TBK1, USP22, ZHX2, GAL, CYP19A1, EDN1, CYP1B1, MBL3P, CYP2C18, NQO1, ICMT, PALLD, CYP2C19, MYC, MPC1, BIRC3, STPG4, AGER, PTF1A, SEMA3D, CRYBG1, ALB, PLB1, SUFU, ARG1, SLC24A4, NLRP3, EGLN3, ARG2, ARNTL, FAM83H, CELIAC2, PARP1, ACTC1, MIRLET7C, MIR143, MIR155, MIR21, MIR135B, MIR499A, CXADRP1, MIR365A, C20orf181, CD24, TPTEP2-CSNK1E, MTCO2P12, LOC110806262, ARR3, STS, ARSD, CD40, CSNK1E, DLL4, CSK, DYM, CSF2, CRY2, CRY1, TIPIN, COL11A2, CCR5, UBE2C, CHRNA4, CFTR, CD44, CD14, ART3, RUNX3, CASR, SMOC1, CASP3, CASP1, CLEC7A, CALCA, TRPM8, BCL2, AXL, TRPM3, CPEB4, ATM, ITCH, FBXW7, FASN, RALBP1, LGALS3, PTGIR, QSOX1, PVT1, KRT19, RAB2A, KRT10, KDR, RAF1, KDM5A, KCNA2, RET, ITGB4, ROCK1, ITGAM, ITGA5, IL17A, CXCL5, STIL, IL10, CXCR2, SLC6A4, SMARCA1, SMPD2, IL2, SOX9, SPARC, SPG7, IGF1, SSRP1, PTGER4, PRTN3, DLC1, LGALS9, COX2, MSX2, CEACAM6, NCL, NEDD9, NEK2, NFATC1, MMP2, CCN3, NRDC, OPRD1, REG3A, MAA, PDCD1, PER1, CYP4F3, PF4, PGF, PIM1, PLA2G1B, LPA, PLAT, PLG, PTPA, PRKAR1A, LMO1, MAPK1, MAP2K7, PRSS2, STAT1, STAT3, IDH1, ID1, RIPK1, TNFRSF10B, NRP1, KAT2B, PER2, SLC16A4, SLC16A3, DCLK1, AURKB, MTA2, KLF4, FAP, SLIT2, LHX2, ADIPOQ, RASAL2, PTGES, CLOCK, MATR3, DLEC1, NR1I3, CHAF1A, ABCB6, F3, ERBB3, NAMPT, TRIM13, EPO, EPHB2, BECN1, DYNLL1, RFXANK, GLI2, TNC, HNF1A, ZEB1, FOXA2, HMOX1, HMGB1, TGM2, GSK3B, TPO, NR2C2, GSK3A, TYR, GLS, UQCRFS1, CYP4F2, UROD, VAV1, VWF, GLB1, XRCC1, YWHAZ, LEPQTL1, CXCR4, GAS6, MIA, USP11, ULK1, RECK, H3P10
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Dysplastic Nevus
Wikipedia
People with a personal or family history of skin cancer or of dysplastic nevus syndrome (multiple atypical moles) should see a dermatologist at least once a year to be sure they are not developing melanoma. ... If this is not mentioned, usually a dermatologist or clinician will require further surgery if moderate to severe cytologic atypia is present – and if residual nevus is present at the surgical margin. Dysplastic nevus syndrome [ edit ] Main article: Dysplastic nevus syndrome "Dysplastic nevus syndrome" refers to individuals who have high numbers of benign moles and also have dysplastic nevi. A small percent of these individuals are members of melanoma kindreds. [12] Inherited dysplastic nevus syndrome is an autosomal dominant hereditary condition. ... Retrieved 18 July 2015 . ^ " dysplastic nevus syndrome " at Dorland's Medical Dictionary ^ Pampena R, Kyrgidis A, Lallas A, Moscarella E, Argenziano G, Longo C (2017). ... "Inheritance of nevus number and size in melanoma and dysplastic nevus syndrome kindreds" . J Natl Cancer Inst . 83 (23): 1726–33. doi : 10.1093/jnci/83.23.1726 .CDK4, CDKN2A, BRAF, NRAS, H3P10, CCND1, MC1R, TP53, CTSD, MIR211, CD82, CDK6, GSTT1, CXCL1, XRCC1, STAT3, TCHH, KAT5, RECQL4, TRH, TNF, BCL2, TGFA, TERT, PRAME, TERF2, SSX2, SOX4, FSCN1, SMARCB1, PMEL, SCN8A, S100A8, U2AF2, LRIT1, AMACR, SESN2, SSX2B, MIR21, MIR144, MIR106B, MIRLET7B, MIA3, KRT25, TNS4, RNASE7, SHCBP1, CADM1, FBXW7, ING3, RTEL1, ING4, IL22, GNMT, BBC3, RHCE, BRMS1, S100A7, CLDN11, MAPK1, HLA-B, GSTM1, GHRH, ETS1, EPHB2, EIF4E, EGFR, EDNRB, DUSP3, DRG2, CSF2, COMP, COL9A3, COL9A2, COL9A1, CMM, AR, ARNT, CD1C, CCND3, HCL2, HNRNPK, PIN1, IGFBP7, PAM, BRCA1, OSM, AQP1, NME1, MSH2, MRC1, MMP13, MMP2, MMP1, MLH1, MIF, MDM2, LGALS3, LGALS1, LAMC2, IL18, IL13, IL1B, APOE
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Brachydactyly, Type B2
Omim
Lehmann et al. (2007) suggested that the disorder in the kindred reported by Herrmann (1974) and some of the patients reported by Maroteaux et al. (1972) as a form of multiple synostoses syndrome (see 186500) may have been the same as BDB2. ... INHERITANCE - Autosomal dominant SKELETAL Hands - Variable terminal deficiency of fingers - Hypoplastic distal phalanges (fingers II-V, mild phenotype) - Absent distal and absent/hypoplastic middle phalanges - (fingers IV and V more severely affected than fingers II and III, intermediate phenotype) - Absent distal and middle phalanges (severe phenotype) - Proximal interphalangeal joint fusion (symphalangism) - Short first metacarpal - Proximally placed thumb - Cutaneous syndactyly - Carpal bone fusion Feet - Variable terminal deficiency of toes - Tarsal bone fusion SKIN, NAILS, & HAIR Skin - Cutaneous syndactyly MISCELLANEOUS - Allelic to proximal symphalangism ( 185800 ), multiple synostoses syndrome 1 ( 186500 ), tarsal-carpal coalition syndrome ( 186570 ), and stapes ankylosis syndrome without symphalangism ( 184460 ) MOLECULAR BASIS - Caused by mutation in the human homolog of the mouse noggin gene (NOG, 602991.0012 ) ▲ Close
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Discoid Fibromas, Familial Multiple
Omim
FMDF is similar to, but histologically and genetically distinct from, Birt-Hogg-Dube syndrome (BHD; 135150), which is characterized by fibrofolliculomas as well as renal and pulmonary cysts. ... Starink et al. (1985) considered the disorder to be distinct from autosomal dominant fibrofolliculomas with trichodiscomas and acrochordons (Birt-Hogg-Dube syndrome). Starink et al. (2012) evaluated 9 families with familial multiple discoid fibromas, including the family reported by Starink et al. (1985), 3 families previously reported by Leter et al. (2008) as having Birt-Hogg-Dube syndrome (families 11, 17, and 20), 3 families from the same village in the Netherlands, and 2 newly ascertained families. Some of the families were referred for evaluation of suspected Birt-Hogg-Dube syndrome. Most patients showed multiple skin-colored, firm, flat, and dome-shaped papules on the pinnae and the central area of the face; lesions on the trunk and limbs were less common.
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Pheochromocytoma-Paraganglioma
Orphanet
For instance, gastrointestinal stromal tumors in patients with Carney-Stratakis syndrome. Etiology About 40% of PPGL occur in the context of an autosomal inherited syndrome. ... Differential diagnosis In patients with paroxysmal symptoms, main differential diagnoses are panic disorder, hot flashes, carcinoid syndrome. Antenatal diagnosis Prenatal diagnosis is not performed except for patients with VHL disease. ... Genetic counseling Genetic testing is recommended for all patients diagnosed with PPGL because 40% of cases occur in the context of an autosomal inherited syndrome. Moreover, patient follow-up is adapted according to the mutated gene (for example, intensive follow-up for SDHB mutation because the risk of malignancy is increased).
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Autosomal Recessive Primary Microcephaly
Orphanet
Epidemiology Exact prevalence of non-syndromic microcephaly is not known. MCPH is more common in Asian and Middle Eastern populations than in Caucasians, in whom an annual incidence of 1/1,000,000 is reported. ... Some carry mutations in one of the genes of Meier-Gorlin syndrome (see this term), i.e. CDC6, CDT1, ORC1, ORC4, ORC6 . ... Differential diagnosis MCPH and Seckel syndrome belong to a clinical continuum, as mutations of some genes ( CENPJ, CEP152 ) result in either phenotype. ... Normal fundus examination is important to distinguish MCPH from the microcephaly-chorioretinopathy syndromes. MRI is crucial to distinguish MCPH from other disorders with congenital microcephaly, such as lissencephaly, Norman-Roberts type (see this term) or infectious embryofetopathies.
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Acth-Independent Macronodular Adrenal Hyperplasia 2
Omim
Description ACTH-independent macronodular adrenal hyperplasia-2 is an autosomal dominant tumor susceptibility with syndromic incomplete penetrance, as a second hit to the ARMC5 gene is required to develop macronodular hyperplasia (Assie et al., 2013). ... Fifteen patients had clinical Cushing syndrome and 3 had subclinical Cushing syndrome. ... All patients carrying a clearly pathogenic ARMC5 mutation had clinical Cushing syndrome, compared with 14 (52%) of 27 of those without mutations or with benign mutations in ARMC5.
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Blastomycosis-Like Pyoderma
Wikipedia
External links [ edit ] Classification D ICD - 10 : L10.1 ( ILDS L10.120) External resources eMedicine : article/1055728 v t e Bacterial skin disease Gram +ve Firmicutes Staphylococcus Staphylococcal scalded skin syndrome Impetigo Toxic shock syndrome Streptococcus Impetigo Cutaneous group B streptococcal infection Streptococcal intertrigo Cutaneous Streptococcus iniae infection Erysipelas / Chronic recurrent erysipelas Scarlet fever Corynebacterium Erythrasma Listeriosis Clostridium Gas gangrene Dermatitis gangrenosa Mycoplasma Erysipeloid of Rosenbach Actinobacteria Mycobacterium-related: Aquarium granuloma Borderline lepromatous leprosy Borderline leprosy Borderline tuberculoid leprosy Buruli ulcer Erythema induratum Histoid leprosy Lepromatous leprosy Leprosy Lichen scrofulosorum Lupus vulgaris Miliary tuberculosis Mycobacterium avium-intracellulare complex infection Mycobacterium haemophilum infection Mycobacterium kansasii infection Papulonecrotic tuberculid Primary inoculation tuberculosis Rapid growing mycobacterium infection Scrofuloderma Tuberculosis cutis orificialis Tuberculosis verrucosa cutis Tuberculous cellulitis Tuberculous gumma Tuberculoid leprosy Cutaneous actinomycosis Nocardiosis Cutaneous diphtheria infection Arcanobacterium haemolyticum infection Group JK corynebacterium sepsis Gram -ve Proteobacteria α: Endemic typhus Epidemic typhus Scrub typhus North Asian tick typhus Queensland tick typhus Flying squirrel typhus Trench fever Bacillary angiomatosis African tick bite fever American tick bite fever Rickettsia aeschlimannii infection Rickettsialpox Rocky Mountain spotted fever Human granulocytotropic anaplasmosis Human monocytotropic ehrlichiosis Flea-borne spotted fever Japanese spotted fever Mediterranean spotted fever Flinders Island spotted fever Verruga peruana Brill–Zinsser disease Brucellosis Cat-scratch disease Oroya fever Ehrlichiosis ewingii infection β: Gonococcemia / Gonorrhea / Primary gonococcal dermatitis Melioidosis Cutaneous Pasteurella hemolytica infection Meningococcemia Glanders Chromobacteriosis infection γ: Pasteurellosis Tularemia Vibrio vulnificus Rhinoscleroma Haemophilus influenzae cellulitis Pseudomonal pyoderma / Pseudomonas hot-foot syndrome / Hot tub folliculitis / Ecthyma gangrenosum / Green nail syndrome Q fever Salmonellosis Shigellosis Plague Granuloma inguinale Chancroid Aeromonas infection ε: Helicobacter cellulitis Other Syphilid Syphilis Chancre Yaws Pinta Bejel Chlamydia infection Leptospirosis Rat-bite fever Lyme disease Lymphogranuloma venereum Unspecified pathogen Abscess Periapical abscess Boil/furuncle Hospital furunculosis Carbuncle Cellulitis Paronychia / Pyogenic paronychia Perianal cellulitis Acute lymphadenitis Pilonidal cyst Pyoderma Folliculitis Superficial pustular folliculitis Sycosis vulgaris Pimple Ecthyma Pitted keratolysis Trichomycosis axillaris Necrotizing fascitis Gangrene Chronic undermining burrowing ulcers Fournier gangrene Elephantiasis nostras Blistering distal dactylitis Botryomycosis Malakoplakia Gram-negative folliculitis Gram-negative toe web infection Pyomyositis Blastomycosis-like pyoderma Bullous impetigo Chronic lymphangitis Recurrent toxin-mediated perineal erythema Tick-borne lymphadenopathy Tropical ulcer This infection-related cutaneous condition article is a stub .
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Perianal Cellulitis
Wikipedia
Classification D ICD - 10 : L03.3 v t e Bacterial skin disease Gram +ve Firmicutes Staphylococcus Staphylococcal scalded skin syndrome Impetigo Toxic shock syndrome Streptococcus Impetigo Cutaneous group B streptococcal infection Streptococcal intertrigo Cutaneous Streptococcus iniae infection Erysipelas / Chronic recurrent erysipelas Scarlet fever Corynebacterium Erythrasma Listeriosis Clostridium Gas gangrene Dermatitis gangrenosa Mycoplasma Erysipeloid of Rosenbach Actinobacteria Mycobacterium-related: Aquarium granuloma Borderline lepromatous leprosy Borderline leprosy Borderline tuberculoid leprosy Buruli ulcer Erythema induratum Histoid leprosy Lepromatous leprosy Leprosy Lichen scrofulosorum Lupus vulgaris Miliary tuberculosis Mycobacterium avium-intracellulare complex infection Mycobacterium haemophilum infection Mycobacterium kansasii infection Papulonecrotic tuberculid Primary inoculation tuberculosis Rapid growing mycobacterium infection Scrofuloderma Tuberculosis cutis orificialis Tuberculosis verrucosa cutis Tuberculous cellulitis Tuberculous gumma Tuberculoid leprosy Cutaneous actinomycosis Nocardiosis Cutaneous diphtheria infection Arcanobacterium haemolyticum infection Group JK corynebacterium sepsis Gram -ve Proteobacteria α: Endemic typhus Epidemic typhus Scrub typhus North Asian tick typhus Queensland tick typhus Flying squirrel typhus Trench fever Bacillary angiomatosis African tick bite fever American tick bite fever Rickettsia aeschlimannii infection Rickettsialpox Rocky Mountain spotted fever Human granulocytotropic anaplasmosis Human monocytotropic ehrlichiosis Flea-borne spotted fever Japanese spotted fever Mediterranean spotted fever Flinders Island spotted fever Verruga peruana Brill–Zinsser disease Brucellosis Cat-scratch disease Oroya fever Ehrlichiosis ewingii infection β: Gonococcemia / Gonorrhea / Primary gonococcal dermatitis Melioidosis Cutaneous Pasteurella hemolytica infection Meningococcemia Glanders Chromobacteriosis infection γ: Pasteurellosis Tularemia Vibrio vulnificus Rhinoscleroma Haemophilus influenzae cellulitis Pseudomonal pyoderma / Pseudomonas hot-foot syndrome / Hot tub folliculitis / Ecthyma gangrenosum / Green nail syndrome Q fever Salmonellosis Shigellosis Plague Granuloma inguinale Chancroid Aeromonas infection ε: Helicobacter cellulitis Other Syphilid Syphilis Chancre Yaws Pinta Bejel Chlamydia infection Leptospirosis Rat-bite fever Lyme disease Lymphogranuloma venereum Unspecified pathogen Abscess Periapical abscess Boil/furuncle Hospital furunculosis Carbuncle Cellulitis Paronychia / Pyogenic paronychia Perianal cellulitis Acute lymphadenitis Pilonidal cyst Pyoderma Folliculitis Superficial pustular folliculitis Sycosis vulgaris Pimple Ecthyma Pitted keratolysis Trichomycosis axillaris Necrotizing fascitis Gangrene Chronic undermining burrowing ulcers Fournier gangrene Elephantiasis nostras Blistering distal dactylitis Botryomycosis Malakoplakia Gram-negative folliculitis Gram-negative toe web infection Pyomyositis Blastomycosis-like pyoderma Bullous impetigo Chronic lymphangitis Recurrent toxin-mediated perineal erythema Tick-borne lymphadenopathy Tropical ulcer This infection-related cutaneous condition article is a stub .
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Lichen Spinulosus
Wikipedia
External links [ edit ] Derm Net NZ Emedicine Thehinhso 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 This condition of the skin appendages article is a stub .