Comprehensive treatment of rare multiple endocrine neoplasia type 1: A case report

BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a rare hereditary disorder caused by mutations of the MEN1 gene. It is characterized by hyperparathyroidism and involves the pancreas, anterior pituitary, duodenum, and adrenal gland. Here, we report a 40-year-old male patient with MEN1 who f...

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Detalles Bibliográficos
Autores principales: Ma, Chen-Hui, Guo, Huai-Bin, Pan, Xin-Yan, Zhang, Wan-Xing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322426/
https://www.ncbi.nlm.nih.gov/pubmed/32607345
http://dx.doi.org/10.12998/wjcc.v8.i12.2647

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322426/
https://www.ncbi.nlm.nih.gov/pubmed/32607345
http://dx.doi.org/10.12998/wjcc.v8.i12.2647

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