| Literature DB >> 3561948 |
Abstract
Familial iridoschisis is a rare ocular disease and is probably transmitted as an autosomal dominant trait. The underlying abnormalities are not understood. Family members should be screened for this condition as well as for associated ocular abnormalities, namely presenile cataracts and narrow anterior chamber angle.Entities:
Mesh:
Year: 1986 PMID: 3561948 DOI: 10.3109/13816818609004131
Source DB: PubMed Journal: Ophthalmic Paediatr Genet ISSN: 0167-6784