Piebaldism
Hazan, C.
Dermatology Online Journal 11(4): 18
2005
ISSN/ISBN: 1087-2108 PMID: 16403390 Document Number: 589233
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.