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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