1.
Ophthalmic Genet
; 39(3): 377-379, 2018 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29377746
RESUMO
Peroxisomal biogenesis disorders are caused by disruption of long chain fatty acid metabolism due to mutations in PEX genes. Individuals with these disorders often have vision loss due to optic atrophy and pigmentary retinopathy. We report an unusual retinal manifestation of peroxisomal biogenesis disorder.