Piebaldism: A rare presentation in Nepalese context
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Keywords

Autosomal dominant
Hypopigmentation
Piebaldism

How to Cite

Bhattarai, S., Maskey, S., & Joshi, A. (2014). Piebaldism: A rare presentation in Nepalese context. Journal of Kathmandu Medical College, 3(2), 88–91. Retrieved from https://jkmc.com.np/ojs3/index.php/journal/article/view/733

Abstract

Piebaldism is a rare autosomal dominant disorder characterised by a congenital white forelock and multiple symmetrical hypopigmented or depigmented macules. We present a case of an 18 year old male with a typical clinical presentation, followed by a co

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