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PubMed · 16403390

Piebaldism.

Carole Hazan
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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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Carole Hazan. 2005-12-30. Piebaldism.. https://pubmed.ncbi.nlm.nih.gov/16403390/

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