Piebaldism: A brief report and review of the literature
- PMID: 23130293
- DOI: 10.4103/2229-5178.96722
Piebaldism: A brief report and review of the literature
Retraction in
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Retraction: Piebaldism: A Brief Report and Review of the Literature.Indian Dermatol Online J. 2024 Apr 29;15(3):569. doi: 10.4103/idoj.idoj_305_24. eCollection 2024 May-Jun. Indian Dermatol Online J. 2024. PMID: 38845665 Free PMC article.
Abstract
Piebaldism is a rare autosomal dominant disorder of melanocyte development characterized by a congenital white forelock and multiple symmetrical stable hypopigmented or depigmented macules. We report a family with piebaldism affecting three successive generations and also review the literature.
Keywords: Autosomal dominant; piebaldism; pigmentary disorder.
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