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CME
Continuing Medical Education
Piebaldism: A Case Report and a Concise Review of the Literature
Janjua SA, Khachemoune A, Guldbakke KK
Cutis
. 2007;80:411-414.
Piebaldism is a rare autosomal dominant disorder characterized by congenital poliosis and leukoderma. We present a case of a 10-year-old girl with a typical clinical presentation, followed by a concise review of the literature discussing the etiology, clinical features, diagnosis, and management of the condition.
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