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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Detalhes bibliográficos
Publicado no:Med Oral Patol Oral Cir Bucal
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Medicina Oral S.L. 2018
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5911358/
https://ncbi.nlm.nih.gov/pubmed/29476668
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4317/medoral.21437
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