Spontaneous repigmentation in an infant with piebaldism
Author:
Affiliation:
1. Section of Dermatology; Hospital General Universitario; Alicante Spain
Publisher
Wiley
Subject
Dermatology
Reference6 articles.
1. Analysis of KIT, SCF, and initial screening of SLUG in patients with piebaldism;Murakami;J Invest Dermatol,2005
2. Piebaldism;Oiso;J Dermatol,2013
3. New KIT mutations in patients with piebaldism;Murakami;J Dermatol Sci,2004
4. Familial case of piebaldism with regression of white forelock;Matsunaga;Clin Exp Dermatol,2008
5. Repigmentation of leukoderma in a piebald patient associated with a novel c-KIT gene mutation, G592E, of the tyrosine kinase domain;Arase;J Dermatol Sci,2011
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3. The color of skin: white diseases of the skin, nails, and mucosa;Clinics in Dermatology;2019-09
4. Extending the Mathematical Palette for Developmental Pattern Formation: Piebaldism;Bulletin of Mathematical Biology;2019-01-28
5. In-frame Val 216 -Ser 217 deletion of KIT in mild piebaldism causes aberrant secretion and SCF response;Journal of Dermatological Science;2018-07
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