Cargando…
Piebaldism Associated with Café-au-lait Macules and Intertriginous Freckling: A Case Report and Review of the Literature
We present 9-year-old fraternal twins from a family with piebaldism, having congenital depigmented macules and meeting the diagnostic criteria for neurofibromatosis type 1 (NF1) due to the multiple café-au-lait macules (CALMs) and intertriginous freckling at the same time. It's still a debatabl...
Autores principales: | Akarsu, Sevgi, İlknur, Turna, Avcı, Ceylan, Fetil, Emel |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Dermatological Association; The Korean Society for Investigative Dermatology
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992560/ https://www.ncbi.nlm.nih.gov/pubmed/33911651 http://dx.doi.org/10.5021/ad.2019.31.5.567 |
Ejemplares similares
-
A novel missense KIT mutation causing piebaldism in one Chinese family associated with café-au-lait macules and intertriginous freckling
por: Jia, Wei-Xue, et al.
Publicado: (2015) -
Piebaldism with multiple café-au-lait–like hyperpigmented macules and inguinal freckling caused by a novel KIT mutation
por: Nagaputra, Jerry C., et al.
Publicado: (2018) -
KIT Gene Mutation Causing Piebaldism Associated with Multiple Café Au-Lait Like Macules and Freckling: Delineating a Cause of this Coexistence
por: Hegde, Shibhani S., et al.
Publicado: (2022) -
Piebaldism with café‐au‐lait macules resulting from a novel mutation of KIT gene in a three‐generation Chinese family
por: Li, Xiaorong, et al.
Publicado: (2023) -
Plexiform Neurofibroma Overlying Giant Café-au-lait Macule
por: Choudhary, Sanjiv V., et al.
Publicado: (2017)