Fig. 2: Clinical diagnoses of 773 patients with inherited eye diseases in Argentina. | npj Genomic Medicine

Fig. 2: Clinical diagnoses of 773 patients with inherited eye diseases in Argentina.

From: Nationwide genetic analysis of more than 600 families with inherited eye diseases in Argentina

Fig. 2: Clinical diagnoses of 773 patients with inherited eye diseases in Argentina.

RP retinitis pigmentosa, EOSRD early-onset severe retinal dystrophy, MD macular dystrophy, CHM choroideremia, CORD cone-rod dystrophy, IRD inherited retinal dystrophy, BBS Bardet–Biedl syndrome, FEVR familial exudative vitreoretinopathy, XLRS X-linked retinoschisis, MAC microphthalmia-anophthalmia-coloboma spectrum, PHPV persistent hyperplastic primary vitreous, CSNB congenital stationary night blindness, PPRCA pigmented paravenous retinochoroidal atrophy, OA optic atrophy. Albinism & related conditions include oculo-cutaneous albinism, ocular albinism, and foveal hypoplasia.

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