Human piebaldism is an expression of neural crest component abnormality that is classically inherited dominantly and is probably heterogeneous genetically. Though usually a stable cutaneous condition,...
Piebaldism is a rare, congenital, autosomal dominant inherited pigmentary disorder, characterized by a white forelock and freckled depigmentation of the forehead, chin, ventral trunk and extremities. ...
A family in which piebaldism is inherited in a dominant pattern is described. In this kindred the cutaneous signs were associated to a high incidence of cancer. Malignancy usually became apparent in t...