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BRIEF REPORT
Year : 2012  |  Volume : 3  |  Issue : 2  |  Page : 144-147

Piebaldism: A brief report and review of the literature


Department of Skin and VD, Government Medical College, Haldwani (Nainital), Uttarakhand, India

Correspondence Address:
Saurabh Agarwal
Department of Skin and VD, Government Medical College, Haldwani (Nainital), Uttarakhand - 263 139
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2229-5178.96722

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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.


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