| Literature DB >> 10994447 |
J B Moloney1, J Blake, B Denham, D Mooney.
Abstract
Two siblings with total regional choroidal atrophy and other manifestations of ectodermal dysplasia are presented. The mode of inheritance is uncertain, but mild macular disease in the father may represent heterozygote manifestation of a recessive condition.Entities:
Mesh：
Year: 1988 PMID： 10994447 DOI： 10.1111/j.1755-3768.1988.tb04596.x
Source DB: PubMed Journal: Acta Ophthalmol (Copenh) ISSN： 0001-639X