| Literature DB >> 22733289 |
A Rosentreter1, S Gaki, S Dinslage, T S Dietlein.
Abstract
Propionic acidemia (PA) is a rare autosomal recessive disorder resulting from deficiency of the biotin-dependent enzyme propionyl-CoA carboxylase, which is necessary for the catabolism of branched chain amino acids and odd-chain fatty acids. Although optic atrophy was documented in four cases, no glaucomatous optic atrophy has yet been described. This article describes the first case of a 12-year-old boy with PA showing bilateral glaucomatous optic disc atrophy due to dysgenetic changes of the angle of the anterior chamber.Entities:
Mesh:
Year: 2012 PMID: 22733289 DOI: 10.1007/s00347-012-2596-x
Source DB: PubMed Journal: Ophthalmologe ISSN: 0941-293X Impact factor: 1.059