Piebaldism with café‐au‐lait macules resulting from a novel mutation of KIT gene in a three‐generation Chinese family

BACKGROUND: Piebaldism is a rare, autosomal dominant, and congenital pigmentary disorder characterized by stable depigmentation of the skin and white forelock. Mutations in KIT or SLUG genes result in piebaldism. Most individuals with piebaldism have a family history of the disorder. METHODS: In thi...

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Detalles Bibliográficos
Autores principales: Li, Xiaorong, Xing, Xiaojing, Liang, Xiaoqiang, Song, Cuihao, Yang, Jie, Ren, Dan, Zhou, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10209842/
https://www.ncbi.nlm.nih.gov/pubmed/37357653
http://dx.doi.org/10.1111/srt.13352

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10209842/
https://www.ncbi.nlm.nih.gov/pubmed/37357653
http://dx.doi.org/10.1111/srt.13352

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