alexa Abstract | Piebaldism: A Brief Report

Dermatology Case Reports
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Piebaldism is an autosomal dominant congenital pigmentary disorder. It is characterised by white forelock and multiple symmetrical stable depigmented macules. We report a familial case of piebaldism affecting a 6 year old female and her father

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Author(s): Kaushik M , Gupta S and Mahendra A


Piebaldism, Autosomal dominant, Pigmentary disorder, Vitiligo, Immunodermatology, Dermatological Oncology, Dermatolgical Medicine

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