A Novel Missense MEN1 Mutation in a Sporadic Case of Multiple Endocrine Neoplasia Type 1 Complicated with Papillary Thyroid Carcinoma

Multiple endocrine neoplasia type 1 (MEN1) is a rare genetic disorder, resulting from MEN1 gene abnormalities, which causes tumors mainly in the endocrine glands. We experienced a sporadic case of MEN1 complicated with papillary thyroid carcinoma (PTC) and found a novel missense mutation in the pati...

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Detalles Bibliográficos
Autores principales: Shibuya, Koji, Ebihara, Ken, Takahashi, Manabu, Kurashina, Tomoyuki, Nagashima, Shuichi, Okada, Kenta, Ishibashi, Shun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Medical Association 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10169261/
https://www.ncbi.nlm.nih.gov/pubmed/37179722
http://dx.doi.org/10.31662/jmaj.2022-0187

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10169261/
https://www.ncbi.nlm.nih.gov/pubmed/37179722
http://dx.doi.org/10.31662/jmaj.2022-0187

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