| Literature DB >> 27320016 |
Ariane Chappaz1, Daniel Barthelmes1, Lorenz Buser2, Jens Funk1, Christina Gerth-Kahlert3.
Abstract
Aicardi syndrome is a rare X-linked cerebro-retinal disorder characterized by agenesis or dysgenesis of the corpus callosum, seizures, and chorioretinal lacunae; microphthalmia or optic nerve coloboma may also be observed. We report the case of an infant born with severe ocular malformations, including an anterior chamber cyst in one eye, which was surgically removed.Entities:
Mesh:
Year: 2016 PMID: 27320016 DOI: 10.1016/j.jaapos.2016.03.016
Source DB: PubMed Journal: J AAPOS ISSN: 1091-8531 Impact factor: 1.220