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Article

Should genetic testing be performed in each patient with sporadic pheochromocytoma at presentation?

European journal of endocrinology - 1 Feb 2009

Pigny Pascal, Cardot-Bauters Catherine, Do Cao Christine, Vantyghem Marie Christine, Carnaille Bruno, Pattou François, Caron Philippe, Wemeau Jean-Louis, Porchet Nicole

Abstract excerpt

BACKGROUND: According to previous studies, around 15% of patients with an apparently sporadic pheochromocytoma and a negative family history had a hereditary disease. This high frequency together with the financial support provided to reference laboratories of molecular genetics by the French government led to a nearly systematic screening in each patient with a pheochromocytoma. OBJECTIVE: To check the...

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Source

Identifiers

PMID: 19029228
DOI: 10.1530/EJE-08-0574

Genes

RET
SDHB
SDHC
SDHD
VHL

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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