Multiple endocrine neoplasia type 1 with neuroglycopenic symptoms with a novel heterozygous MEN1 gene mutation

Multiple endocrine neoplasia type 1 with neuroglycopenic symptoms with a novel heterozygous MEN1 gene mutation

Abstract Background Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder caused by mutations in the MEN1 gene located on the long arm of chromosome 11. Case presentation. A 32-year-old male was admitted to the Division of Endocrinology with a three-year history of recurrent e...

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Bibliographic Details
Main Authors: Xinchen Jiang, Shixiong Tang, Guoqing Yang, Lite Ge, Fan Peng
Format: Article
Language:English
Published: BMC 2025-07-01
Series:World Journal of Surgical Oncology
Subjects:
Multiple endocrine neoplasia type 1
The MEN1 gene
Parathyroid adenoma
Pancreatic adenoma
Pituitary microadenoma
Online Access:https://doi.org/10.1186/s12957-025-03942-8
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https://doi.org/10.1186/s12957-025-03942-8

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