Clinical features and molecular genetic analysis in a Turkish family with oral white sponge nevus

BACKGROUND: Oral white sponge nevus (WSN) is a rare autosomal dominant benign condition, characterized by asymptomatic spongy white plaques. Mutations in Keratin 4 (KRT4) and 13 (KRT13) have been shown to cause WSN. Familial cases are uncommon due to irregular penetrance. Thus, the aim of the study...

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Detalles Bibliográficos
Autores principales: Kürklü, Esma, Öztürk, Şükrü, Cassidy, Andrew J., Ak, Gülsüm, Koray, Meltem, Çefle, Kıvanç, Palandüz, Şükrü, Güllüoğlu, Mine G, Tanyeri, Hakkı, McLean, William-Henry-Irwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medicina Oral S.L. 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5911358/
https://www.ncbi.nlm.nih.gov/pubmed/29476668
http://dx.doi.org/10.4317/medoral.21437

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5911358/
https://www.ncbi.nlm.nih.gov/pubmed/29476668
http://dx.doi.org/10.4317/medoral.21437

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