A New Locus for Congenital Cataract, Microcornea, Microphthalmia, and Atypical Iris Coloboma Maps to Chromosome 2

Objective: To report a novel phenotype of autosomal dominant atypical congenital cataract associated with variable expression of microcornea, microphthalmia, and iris coloboma linked to chromosome 2. Molecular analysis of this phenotype may improve our understanding of anterior segment development.


Published in:
Ophthalmology, 116, 154-162
Year:
2009
Keywords:
Laboratories:




 Record created 2010-11-30, last modified 2018-09-13


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