| Literature DB >> 2078126 |
M Mathieu1, E Bourges, F Caron, C Piussan.
Abstract
Waardenburg syndrome type I is transmitted as an autosomal dominant trait. The main features are dystopia canthorum, partial pigmentary disorder and perceptive deafness. Osteo-articular and intestinal malformations may be observed. In an affected family, the unusual combination of Waardenburg syndrome and severe congenital heart disease has been observed in a child.Entities:
Mesh:
Year: 1990 PMID: 2078126
Source DB: PubMed Journal: Arch Fr Pediatr ISSN: 0003-9764