Bilateral persistent fetal vasculature due to a mutation in the Norrie disease protein gene
Payabvash S, Anderson JS, Nascene DR. Bilateral persistent fetal vasculature due to a mutation in the Norrie disease protein gene. The Neuroradiology Journal 2015, 28: 623-627. PMID: 26459204, PMCID: PMC4757132, DOI: 10.1177/1971400915609350.Peer-Reviewed Original ResearchMeSH KeywordsBlindnessEye ProteinsGenetic Diseases, X-LinkedHumansInfantMagnetic Resonance ImagingMaleMutationNerve Tissue ProteinsNervous System DiseasesOptic DiskPersistent Fetal Circulation SyndromeRetinal DegenerationRetinal DiseasesRetinal HemorrhageSpasms, InfantileTomography, X-Ray ComputedVitreous Body