| Literature DB >> 3355418 |
J F Salmon1, C E Wallis, A D Murray.
Abstract
Autosomal dominant microcornea with a cataract, previously described in four families, was documented in a seven-generation family. Eighteen family members had microcornea and a cataract, and an additional six had sclerocornea or Peters' anomaly. Most individuals with microcornea had a corneal diameter of less than 11 mm in both meridians, with moderately steep corneal curvatures. The inherited cataract progressed to form a total cataract after visual maturity had been achieved. In the four affected children who had not undergone cataract extraction, the common abnormality was a posterior polar lens opacity. The variability of expressivity of the dominant gene would suggest that the embryological origins of microcornea and sclerocornea are similar.Entities:
Mesh:
Year: 1988 PMID: 3355418 DOI: 10.1001/archopht.1988.01060130551034
Source DB: PubMed Journal: Arch Ophthalmol ISSN: 0003-9950