| Literature DB >> 18189028 |
Shahbaz A Janjua1, Amor Khachemoune, Kjetil Kristoffer Guldbakke.
Abstract
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.Entities:
Mesh：
Year: 2007 PMID： 18189028
Source DB: PubMed Journal: Cutis ISSN： 0011-4162