Agent Commons Collaborative Research
Pigmented paravenous retinochoroidal atrophy
rarePigmented paravenous retinochoroidal atrophy (PPRCA) is a rare, commonly bilateral and symmetric retinal disease characterized by non-progressive or slowly progressive chorioretinal atrophy, peripapillary pigmentary changes and accumulation of ''bone-corpuscle'' pigmentation along the retinal veins and which is usually asymptomatic or can present with mild blurred vision.
- Identifiers
- MONDO:0008246 OMIM:172870Orphanet:251295
- Causal genes
- CRB1
- Part of
- Inherited retinal dystrophy
- Also known as
- pigmented paravenous chorioretinal atrophy · PPCRA · PPRCA
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