Repigmentation of White Forelock in a Familial Case of Piebaldism Reported via Teledermatology in the COVID-19 Era

Author:

Gaudiello Francesca,Ferrillo Maria,Vastarella Maria,Fabbrocini Gabriella,Patrì Angela

Abstract

Piebaldism is a rare autosomal dominant disorder characterized by leucoderma with leucotrichia. We describe a case of white forelock repigmentation in an infant with piebaldism, thanks to a photograph sent by the patient’s mother to our dermatology clinic, during COVID-19 pandemic.

Publisher

S. Karger AG

Subject

Dermatology

Reference3 articles.

1. Murakami T, Fukai K, Oiso N. New KIT mutations in patients with piebaldism. J Dermatol Sci. 2004;35(1):29–33.

2. Saleem MD. Biology of human melanocyte development, Piebaldism, and Waardenburg syndrome. Pediatr Dermatol. 2019;36(1):72–84.

3. Matsunaga H, Tanioka M, Utani A, Miyachi Y. Familial case of piebaldism with regression of white forelock. Clin Exp Dermatol. 2008;33(4):511–2.

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