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Article

Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas.

Endocrine-related cancer - 1 Dec 2011

Welander Jenny, Söderkvist Peter, Gimm Oliver

Abstract excerpt

Pheochromocytomas (PCCs) and paragangliomas (PGLs) are rare neuroendocrine tumors of the adrenal glands and the sympathetic and parasympathetic paraganglia. They can occur sporadically or as a part of different hereditary tumor syndromes. About 30% of PCCs and PGLs are currently believed to be caused by germline mutations and several novel susceptibility genes have recently been discovered. The clinical...

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Source

Identifiers

PMID: 22041710
DOI: 10.1530/ERC-11-0170

Genes

EGLN1
MAX
MEN1
SDHA
SDHAF2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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