| Literature DB >> 7573149 |
Abstract
We report on 3 unrelated Brazilian patients with shortness of stature, hypertelorism, eye anomalies, facial clefting, hearing loss, urogenital abnormalities, omphalocele, "caudal appendage," and mental retardation. Two patients were born to normal and non-consanguineous parents and one was born to consanguineous (first cousin) parents (F = 1/16). The similarity of our patients with those previously reported by Malpuech et al. [Am J Med Genet 16:475-480, 1983] led us to suggest that they have the same condition.Entities:
Mesh:
Year: 1995 PMID: 7573149 DOI: 10.1002/ajmg.1320580104
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299