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Case report: Rare oral manifestations in Cowden syndrome with PTEN mutation

BackgroundCowden syndrome (CS) is a rare genetic disorder associated with PTEN gene mutations. It is characterized by macrocephaly, specific mucocutaneous features, and a predisposition to benign and malignant tumors. Cases of CS primarily presenting with oral clinical manifestations are relatively...

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Principais autores: Wei Yuan, Yanbin Liu, Haibin Sun, Ming Su, Lizheng Qin, Xin Huang
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2024-02-01
coleção:Frontiers in Oncology
Assuntos:
Cowden syndrome
PTEN mutation
oral lesions
clinical manifestations
genetic testing
Acesso em linha:https://www.frontiersin.org/articles/10.3389/fonc.2024.1323225/full
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