Revision of Initial Referral Diagnosis after Genotypic Confirmation of Familial Exudative Vitreoretinopathy

Author:

Hudson Julia L.ORCID,da Cruz Natasha F.S.ORCID,Kunkler Anne L.,Carletti PieroORCID,Negron Catherin I.,Berrocal Audina M.ORCID

Funder

VitreoRetinal Surgery Foundation

Research to Prevent Blindness

U.S. Department of Defense

NIH

Publisher

Elsevier BV

Reference7 articles.

1. Mutations in LRP5, FZD4, TSPAN12, NDP, ZNF408, or KIF11 genes account for 38.7% of Chinese patients with familial exudative vitreoretinopathy;Rao;Invest Ophthalmol Vis Sci,2017

2. Complex genetics of familial exudative vitreoretinopathy and related pediatric retinal detachments;Kondo;Taiwan J Ophthalmol,2015

3. High prevalence of peripheral retinal vascular anomalies in family members of patients with familial exudative vitreoretinopathy;Kashani;Ophthalmology,2014

4. Genetic screening of Wnt signaling factors in advanced retinopathy of prematurity;Hiraoka;Mol Vis,2010

5. Genetic variants of FZD4 and LRP5 genes in patients with advanced retinopathy of prematurity;Kondo;Mol Vis,2013

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