Corneal dystrophy - Wikipedia
... dystrophy Meesmann juvenile epithelial corneal dystrophy Gelatinous drop-like corneal dystrophy Lisch epithelial corneal ... mucinous corneal dystrophy Meesmann corneal dystrophy Lisch epithelial corneal dystrophy Gelatinous drop-like corneal dystrophy ... of lattice corneal dystrophy Granular corneal dystrophy, type 1 Granular corneal dystrophy, type 2 Macular corneal dystrophy ... Lattice corneal dystrophy Granular corneal dystrophy Macular corneal dystrophy Schnyder crystalline corneal dystrophy ...
Gardner's syndrome - Wikipedia
Corneal dystrophy (CD) - An overview | Capsule Health
Cogan microcystic dystrophy, and anterior basement membrane dystrophyMeesmann corneal dystrophy (MECD) or juvenile epithelial ... Epithelial basement membrane corneal dystrophy (EBMCD), aka map-finger-dot dystrophy, ... Classification International Classification of Corneal Dystrophies (IC3D) (2015):Sub-classified by the anatomic location ... Meesmann corneal dystrophy (MECD) or juvenile epithelial corneal dystrophy. *Epithelial-stromal or Bowmans CD:*Reis-Bücklers ...
MedlinePlus: Genetic Conditions: J
Juvenile hereditary epithelial dystrophy, see Meesmann corneal dystrophy. *Juvenile hyperuricemia syndrome, see Lesch-Nyhan ... Juvenile retinoschisis, see X-linked juvenile retinoschisis. *Juvenile rheumatoid arthritis, see Juvenile idiopathic arthritis ... Juvenile Pagets disease, see Juvenile Paget disease. *Juvenile pernicious anemia with proteinuria due to selective intestinal ... Juvenile intestinal polyposis, see Juvenile polyposis syndrome. *Juvenile macular degeneration, see Stargardt macular ...
DeCS 2020 - June 23, 2020 version
Juvenile Hereditary Epithelial Dystrophy use Corneal Dystrophy, Juvenile Epithelial of Meesmann Juvenile Hormones ... Juvenile Onset Stills Disease use Arthritis, Juvenile Juvenile Onset Vitelliform Macular Dystrophy use Vitelliform Macular ... Juvenile-Onset Stills Disease use Arthritis, Juvenile Juvenile-Onset Vitelliform Macular Dystrophy use Vitelliform Macular ... Juvenile Neuroaxonal Dystrophy use Neuroaxonal Dystrophies Juvenile Neuronal Ceroid Lipofuscinosis use Neuronal Ceroid- ...
DeCS 2007 - New terms
DeCS 2007 - New terms
DeCS 2007 - New terms
DeCS 2007 - New terms
DeCS 2007 - New terms
DeCS 2007 - New terms
DeCS 2007 - New terms
DeCS 2007 - New terms
DeCS 2007 - New terms
DeCS 2007 - New terms
DeCS 2007 - New terms
Asphyxiating thoracic dysplasia - WikiProjectMed
KRT3 (Meesmann juvenile epithelial corneal dystrophy). *KRT4 (White sponge nevus). *KRT5 (Epidermolysis bullosa simplex) ... "Asphyxiating thoracic dystrophy". Genetics Home Reference. Archived from the original on 2019-07-17. Retrieved 2019-11-14.. ... Jeune M, Beraud C, Carron R (1955). "[Asphyxiating thoracic dystrophy with familial characteristics]". Archives Françaises de ... "Asphyxiating Thoracic Dystrophy (Jeune Syndrome) Treatment & Management: Approach Considerations, Medical Care, Surgical Care" ...
DeCS 2017 - July 04, 2017 version
Juvenile Hereditary Epithelial Dystrophy use Corneal Dystrophy, Juvenile Epithelial of Meesmann Juvenile Hormones ... Juvenile Myoclonic Epilepsy of Janz use Myoclonic Epilepsy, Juvenile Juvenile Neuroaxonal Dystrophy use Neuroaxonal Dystrophies ... Juvenile Onset Stills Disease use Arthritis, Juvenile Juvenile Onset Vitelliform Macular Dystrophy use Vitelliform Macular ... Juvenile-Onset Stills Disease use Arthritis, Juvenile Juvenile-Onset Vitelliform Macular Dystrophy use Vitelliform Macular ...
autosomal dominant | Hereditary Ocular Diseases
Stocker-Holt dystrophy is clinically somewhat similar to Meesmann corneal dystrophy but is caused by a different mutation and ... A rare form of hereditary epithelial dystrophy of the cornea: a genetic, clinical, and pathologic study.. Stocker FW, Holt LB. ... The distinction between juvenile and adult-onset primary open-angle glaucoma. Wiggs JL, Damji KF, Haines JL, Pericak-Vance MA, ... Stocker-Holt dystrophy is caused by mutations in KRT12 (17q12). Like Meesmann dystrophy (122100), it follows an autosomal ...
Meesmann's | Vagelos College of Physicians and Surgeons
Autosomal dominantly inherited and also called juvenile hereditary epithelial dystrophy.. Clinical Features. *Symptoms: * ... Superficial corneal debridement. *Photo therapeutic keratectomy maybe required in patient with severe recurrent erosions or ... Foreign body sensation due to epithelial erosion may occur as the cysts begin to rupture onto the ocular surface ...
Corneal Erosion Syndrome | Ento Key
Said BASICS DESCRIPTION Recurrent corneal erosion syndrome (RCES) is characterized by episodes of spontaneous breakdown of the ... corneal epithelium associated with symptoms ranging from ocular discomfort to severe pain. It is usually unilateral and is ... Meesmanns corneal dystrophy: Intermittent rupture of epithelial microcysts as they reach the surface of the cornea, causing ... Systemic conditions such as epidermolysis bullosa and Juvenile X-linked Alports syndrome have inherent basement membrane ...
MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal
Corneal dystrophy, gelatinous drop-like (C535480) ... Corneal Dystrophy, Juvenile Epithelial of Meesmann (D053559) ... Corneal Dystrophy, Avellino Type ,Granular and lattice corneal dystrophies ,Granular corneal dystrophy type 2 ,Granular Corneal ... ACD ,Avellino corneal dystrophy ,CDA ,CGD2 ,Combined granular-lattice corneal dystrophies ,Combined Granular-Lattice Corneal ... Endothelial Dystrophy, Congenital Hereditary, with Nail Hypoplasia (C565591) ... Epithelial Recurrent Erosion Dystrophy ( ...
herenciageneticayenfermedad: Health Conditions - Genetics Home Reference: M | Published: March 7, 2017
Meesmann corneal epithelial dystrophy, see Meesmann corneal dystrophy. *Meesmann epithelial corneal dystrophy, see Meesmann ... Murray syndrome, see juvenile hyaline fibromatosis. *muscle AMP deaminase deficiency, see adenosine monophosphate deaminase ... Meretoja syndrome, see lattice corneal dystrophy type II. *merosin-deficient muscular dystrophy, see LAMA2-related muscular ... muscular dystrophy due to LAMA2 deficiency, see LAMA2-related muscular dystrophy. *Muscular dystrophy, congenital progressive, ...
Molecular Vision: A novel mutation (p.Glu1389AspfsX16) of the phosphoinositide kinase, FYVE finger containing gene found in a...
... dystrophy) [3], Meesmann corneal dystrophy [4,5], macular corneal dystrophy [6], gelatinous drop-like corneal dystrophy [7], ... corneal epithelial dystrophy. Am J Hum Genet. 1997; 61:1268-75. [PMID: 9399908] ... In both knockout lines, neurologic defects and juvenile or perinatal death was seen. Thus, complete loss of function of the ... related corneal dystrophies (i.e., granular corneal dystrophy, lattice corneal dystrophy type I, granular corneal dystrophy ...
Aniridia
Cas9 genome editing has been used for disease modelling and/or gene therapy for AAK and Meesmanns epithelial corneal dystrophy ... We describe a family with Juvenile onset open angle glaucoma (JOAG), where one of the two children had JOAG and the other ... Examples include epithelial corneal dystrophies, aniridia, ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome, xeroderma ... We recorded the corneal status by slit-lamp examination and classified the corneal abnormalities according to the Mackman, ...
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... corneal dystrophy Lisch epithelial corneal dystrophy Meesmann corneal dystrophy Subepithelial mucinous corneal dystrophy ... Surface wave detection Vision Weberian apparatus Reproduction Bubble nest Clasper Egg case Development Ichthyoplankton Juvenile ... corneal dystrophy Fleck corneal dystrophy Granular corneal dystrophy Lattice corneal dystrophy Macular corneal dystrophy ... Lisch Epithelial Corneal Dystrophy Orphanet Lisch epithelial corneal dystrophy (LECD) is a very rare form of superficial ...