| Literature DB >> 7362812 |
V Feiler-Ofry, V Godel, P Nemet, M Lazar.
Abstract
A 7-year-old boy had an unusual association of median cleft-face syndrome, a characteristic physiognomy, unilateral retinal dysplasia, and bilateral retinal detachment. Despite surgical treatment to both eyes he became blind. The hereditary pattern operating in this complex disorder was found to be consistent with an autosomal dominant trait.Entities:
Mesh:
Year: 1980 PMID: 7362812 PMCID: PMC1039361 DOI: 10.1136/bjo.64.2.121
Source DB: PubMed Journal: Br J Ophthalmol ISSN: 0007-1161 Impact factor: 4.638