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Article

Multiple endocrine neoplasia type 2: 2007 update.

Hormone research - 1 Jan 2007

Raue Friedhelm, Frank-Raue Karin

Abstract excerpt

BACKGROUND: Multiple endocrine neoplasia type 2 (MEN-2) is an autosomal dominant tumour syndrome caused by germline-activating mutations of the RET proto-oncogene. It is clinically characterised by the presence of medullary thyroid carcinoma (MTC), bilateral pheochromocytoma and primary hyperparathyroidism (MEN-2A) within a single patient. Three distinct clinical forms have been described depending on the...

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Identifiers

PMID: 18174721
DOI: 10.1159/000110589

Genes

RET

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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