Cargando…
A novel keratin 13 variant in a four‐generation family with white sponge nevus
We report a novel KRT13 germ line variant that causes white sponge nevus (WSN) with mucosal dysplasia. Genital, vaginal, and cervical WSN were observed in four female patients, of whom two had premalignant cervical lesions at young age. Two of the 12 patients with oral WSN developed oral squamous ce...
Autores principales: | de Haseth, Stephanie B., Bakker, Egbert, Vermeer, Maarten H., el Idrissi, Hakima, Bosse, Tjalling, Smit, Vincent T.H.B.M., Terron‐Kwiatkowski, Anna, McLean, W.H. Irwin, Peters, Alexander A.W., Hes, Frederik J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5582238/ https://www.ncbi.nlm.nih.gov/pubmed/28878914 http://dx.doi.org/10.1002/ccr3.1073 |
Ejemplares similares
-
Keratin 13 mutations associated with oral white sponge nevus in two Chinese families
por: Cai, Wenping, et al.
Publicado: (2014) -
White Sponge Nevus Caused by Keratin 4 Gene Mutation: A Case Report
por: Qiao, Yahui, et al.
Publicado: (2022) -
Melanocytic Nevus in the External Auditory Canal with Keratin Accumulation
por: Jeong, Junhui, et al.
Publicado: (2021) -
Clinical features and molecular genetic analysis
in a Turkish family with oral white sponge nevus
por: Kürklü, Esma, et al.
Publicado: (2018) -
White Sponge Nevus: A Case Report
por: Aghbali, Amirala, et al.
Publicado: (2009)