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Article

Review: Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes?

The Journal of clinical endocrinology and metabolism - 1 Aug 2006

Jiménez Camilo, Cote Gilbert, Arnold Andrew, Gagel Robert F

Abstract excerpt

CONTEXT: The recent identification of germline mutations of the mitochondrial complex II genes in variants of paraganglioma/pheochromocytoma syndrome has enlarged the number of known causative genes for hereditary pheochromocytoma. A question confronting clinicians is whether they should screen patients with apparently sporadic pheochromocytomas for unsuspected germline mutations of some or all of the seven genes...

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Source

Identifiers

PMID: 16735498
DOI: 10.1210/jc.2005-2178

Genes

RET
SDHB
SDHD
VHL
MEN1
SDHC

Provenance

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

Source receipt: pubmed, retrieved 7 Sept 2026.

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