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Article

Novel association of MEN1 gene mutations with parathyroid carcinoma

12 May 2017

Abstract excerpt

Inactivating mutations of the multiple endocrine neoplasia 1 (MEN1) gene cause MEN1 syndrome, characterized by primary hyperparathyroidism (pHPT), and parathyroid and gastro‑entero‑pancreatic pituitary tumors. At present, only 14 cases of malignant parathyroid tumor have been associated with the syndrome, with 6 cases carrying an inactivating mutation of the MEN1 gene. The present study presents the case of a...

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Identifiers

PMID: 28693130
DOI: 10.3892/ol.2017.6162

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