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  • Title: [Waardenburg's syndrome and severe cyanotic cardiopathy].
    Author: Mathieu M, Bourges E, Caron F, Piussan C.
    Journal: Arch Fr Pediatr; 1990 Nov; 47(9):657-9. PubMed ID: 2078126.
    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.
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