Researchers link early cone dysfunction in RPGR-related retinal dystrophy to high myopia, with timing of degeneration ...

Mutations in the PRPH2 gene cause adult-onset macular retinal dystrophy. However, it’s hard to tell which gene is affected. That means the exact cause is unknown.

These include autosomal dominant drusen, Sorsby fundus dystrophy, pachydrusen, late-onset Stargardt disease, extensive macular atrophy with pseudodrusen, pseudoxanthoma elasticum, North Carolina ...

Conditions linked to these abnormalities include retinitis pigmentosa, cone-rod dystrophy, macular diseases and third-branch disorders. The most identified gene mutation was in ABCA4.

Conditions linked to these abnormalities include retinitis pigmentosa, cone-rod dystrophy, macular diseases and third-branch disorders. The most identified gene mutation was in ABCA4.

OKLAHOMA CITY – Researchers at the University of Oklahoma are advancing the fight against inherited retinal diseases (IRDs) with new genetic research that aims to improve diagnoses and lay ...