retinitis pigmentosa type 3 (RP3)

Pathology: - choroidoretinal degeneration Genetics: - mutations in RPGR gene Clinical manifestations: 1) no visual defects 2) scintillating, golden-hued, patchy appearance most apparent around the macula (tapetal-like retinal reflex)

Database Correlations

OMIM correlations MORBIDMAP 312610

References

OMIM :accession 300389, 312610