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Article

Bilateral persistent fetal vasculature due to a mutation in the Norrie disease protein gene.

The neuroradiology journal - 1 Dec 2015

Payabvash Seyedmehdi, Anderson Jill S, Nascene David R

Abstract excerpt

We report a case of a 7-week-old boy with bilateral leukocoria and asymmetric microphthalmia who was found to have Norrie disease. Symmetrically hyperdense globes with no evidence of calcification were seen on CT scan. The MRI showed bilateral retinal hemorrhages resulting in conical vitreous chambers-narrow at the optic disc and widened toward the lens-characteristic of persistent fetal vasculature. Genetic...

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Identifiers

PMID: 26459204
DOI: 10.1177/1971400915609350
PMCID: PMC4757132

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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