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Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies

Fig. 2

Distribution of the phenotypes of 194 North African families with non-syndromic IRD. According to disease categories in the center chart, and within each category in the outer charts. ACHM: achromatopsia, ARB: autosomal recessive bestrophinopathy, BVMD: Best vitelliform macular dystrophy, CHM: choroideremia, CRD: cone-rod dystrophy, CNSB: congenital stationary night blindness, EORD: early onset retinal dystrophy, ESCD: enhanced S-cone syndrome, LCA: Leber congenital amaurosis, OCA: oculocutaneous albinism, RP: retinitis pigmentosa, RPA: retinitis punctata albescens, STGD: Stargardt disease

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172