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Waardenburg's syndrome case report and review of the literature
Proceedings. 1999; 13 (1-2): 35-37
in English | IMEMR | ID: emr-52225
ABSTRACT
A case of Waardenburg syndrome [WS] is described in a 16 year old boy who presented with hetero-chromic irides, congenital deafness, white forelock and piebaldism like hypopigmented macules on dorsum of this hands, forearms and upper right chest since birth
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Index: IMEMR (Eastern Mediterranean) Main subject: Skin / Iris / Piebaldism / Review / Deafness Type of study: Case report Limits: Humans / Male Language: English Journal: Proceedings Year: 1999

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Index: IMEMR (Eastern Mediterranean) Main subject: Skin / Iris / Piebaldism / Review / Deafness Type of study: Case report Limits: Humans / Male Language: English Journal: Proceedings Year: 1999