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FOVEAL HYPOPLASIA 2

Known as: FHONDA, FVH2, FOVEAL HYPOPLASIA 2 WITH OR WITHOUT OPTIC NERVE MISROUTING AND/OR ANTERIOR SEGMENT DYSGENESIS 
National Institutes of Health

Papers overview

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2017
2017
Purpose To refine the Minnesota Grading System (MGS) using definitions from the Age-Related Eye Disease Studies (AREDS) into a… 
2014
2014
Albinism is a rare genetic condition characterized by common visual deficits and a variable hypopigmented phenotype. To date… 
Review
2013
Review
2013
PurposeTo study the pathomorphology of subretinal hemorrhage (SRH) seen in eyes with branch retinal vein occlusion (BRVO) and its… 
2013
2013
Enhanced S-cone syndrome is a rare, slowly progressive autosomal recessively inherited retinal degeneration related to mutations… 
1999
1999
An 8‐month‐old boy with global developmental delay, including visual and hearing inattention, was examined in the ophthalmic… 
Review
1989
Review
1989
The historical development of the foveal electroretinogram is reviewed. The factors required to obtain a local cone…