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Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 11/2018, Volume 256, Issue 11, pp. 2149 - 2156
To describe and analyse the clinical and genetic characteristics of digenic familial exudative vitreoretinopathy (FEVR).The study cohort consisted of patients... 
Phenotype | Digenic FEVR | Ophthalmology | FEVR | Medicine & Public Health | Gene | VARIANTS | FZD4 | LRP5 | OPHTHALMOLOGY | MUTATIONS | SPECTRUM | IDENTIFICATION | Medicine, Experimental | Medical research | Anopheles | Genetic aspects | Analysis | Familial exudative vitreoretinopathy | Phenotypes | Genetic analysis | LRP5 protein | Mutation | Age | Genotypes | Index Medicus
Journal Article
Journal of Glaucoma, ISSN 1057-0829, 01/2018, Volume 27, Issue 1, pp. e1 - e6
We report two cases of bilateral severe familial exudative vitreoretinopathy (FEVR) presenting with bilateral angle closure glaucoma, with evidence of... 
falciform fold | FZD4 | ANGLE-CLOSURE GLAUCOMA | neovascular glaucoma | OPHTHALMOLOGY | secondary glaucoma | familial exudative vitreoretinopathy | Glaucoma | Care and treatment | Genetic disorders | Research | Risk factors
Journal Article
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, ISSN 0146-0404, 06/2019, Volume 60, Issue 7, pp. 2659 - 2666
PURPOSE. The purpose of this study was to investigate the genetic mutation spectrum in Chinese patients with familial exudative vitreoretinopathy-associated... 
next-generation sequencing | FZD4 | genetic mutation spectrum | SURGICAL OUTCOMES | CLINICAL-FEATURES | IDENTIFICATION | TSPAN12 | genotype-phenotype association | rhegmatogenous retinal detachment | ZNF408 | GENES | OPHTHALMOLOGY | LRP5 MUTATIONS | familial exudative vitreoretinopathy | NDP | CHINESE PATIENTS
Journal Article
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 12/2018, Volume 59, Issue 15, pp. 5726 - 5734
Journal Article
Journal Article
Guoji Yanke Zazhi, ISSN 1672-5123, 11/2018, Volume 18, Issue 11, pp. 1978 - 1981
Familial exudative vitreoretinopathy(FEVR)is a rare inherited disorder of retinal angiogenesis. It is characterized by avascular peripheral retina. Mutations... 
treatment | diagnosis | familial exudative vitreoretinopathy
Journal Article
International Ophthalmology, ISSN 0165-5701, 04/2019, Volume 39, Issue 4, pp. 935 - 941
PurposeTo report the identical twins who had mirror fundus and angiographic images of familial exudative vitreoretinopathy (FEVR).Case presentationA pair of 16... 
Familial exudative vitreoretinopathy | Identical twins | Mirror-image phenomenon | OPHTHALMOLOGY | MUTATIONS | Eye diseases | Genetic aspects | Ophthalmology | Twins | Pathogenesis | Images | Disorders | Visual acuity | Genetics | Heredity | Exudation | Children | Acuity | Index Medicus
Journal Article
Journal Article
Journal Article
International Eye Science, ISSN 1672-5123, 12/2017, Volume 17, Issue 12, pp. 2270 - 2273
Familial exudative vitreoretinopathy(FEVR)is a hereditary disease associated with abnormal angiogenesis in the pediatric period. The most prominent finding of... 
Familial exudative vitreoretinopathy | Genes mutation | Vitreoretinopathy | Clinical classification | clinical classification | genes mutation | familial exudative vitreoretinopathy | vitreoretinopathy
Journal Article
Scientific Reports, ISSN 2045-2322, 05/2016, Volume 6, Issue 1, pp. 26564 - 26564
Journal Article
Journal Article
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