KIT gene mutation causing piebaldism associated with multiple Café Au-Lait like macules and freckling: Delineating a cause of this coexistence
Author:
Publisher
Medknow
Subject
Infectious Diseases,Microbiology (medical),Dermatology,Immunology and Allergy
Reference14 articles.
1. Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism;Giebel;Proc Natl Acad Sci U S A,1991
2. Piebaldism: A brief report and review of the literature;Agarwal;Indian Dermatol Online J,2012
3. Piebaldism with multiple café-au-lait–like hyperpigmented macules and inguinal freckling caused by a novel KIT mutation;Nagaputra;JAAD Case Rep,2018
4. Novel mutations and deletions of the KIT (steel factor receptor) gene in human piebaldism;Ezoe;Am J Hum Genet,1995
5. Biology of human melanocyte development, Piebaldism, and Waardenburg syndrome;Saleem;Pediatr Dermatol,2019
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1. KIT Mutation Associated with Depigmented Patches Regression and Multiple Café-au-lait Macules Development in a Patient with Piebaldism: A Case Report;Clinical, Cosmetic and Investigational Dermatology;2024-03
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