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Piebaldism
1Department of Dermatology, New York University School of Medicine, USA.
Dermatology Online Journal
|January 13, 2006
Abstract:
A 46-year-old man presented with a history of a congenital pigment disorder. On physical examination hypopigmented and depigmented patches were present on the mid-forehead, anterior chest, and extremities. He also had loss of pigment of the medial eyebrows and a white forelock. The patient has a family history of a similar congenital pigment disorder, the pattern of which is indicative of the autosomal dominant disorder piebaldism.
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