KIT Gene Mutation Causing Piebaldism Associated with Multiple Café Au-Lait Like Macules and Freckling: Delineating a Cause of this Coexistence

Piebaldism is a rare genetic disorder of congenital leukoderma caused by mutation in KIT proto-oncogene receptor tyrosine kinase. We present a 10-year-old boy with congenital depigmented macules suggestive of piebaldism associated with café au lait macules and skin fold freckling complicating the di...

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Detalles Bibliográficos
Autores principales: Hegde, Shibhani S., Srinivas, Sahana M., Nanjundappa, Nijaguna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115335/
https://www.ncbi.nlm.nih.gov/pubmed/37089832
http://dx.doi.org/10.4103/idoj.idoj_368_22

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