Piebaldism: a case report and a concise review of the literature
- PMID: 18189028
Piebaldism: a case report and a concise review of the literature
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.