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Article

Routine genetic screening with a multi-gene panel in patients with pheochromocytomas.

Endocrine - 1 Jan 2018

Sbardella Emilia, Cranston Treena, Isidori Andrea M, Shine Brian, Pal Aparna, Jafar-Mohammadi Bahram, Sadler Greg, Mihai Radu, Grossman Ashley B

Abstract excerpt

PURPOSE: Several new gene mutations have been reported in recent years to be associated with a risk of familial pheochromocytoma. However, it is unclear as to whether extensive genetic testing is required in all patients. METHODS: The clinical data of consecutive patients operated for pheochromocytoma over a decade in a tertiary referral center were reviewed. Genetic screening was performed using a 10-gene panel:...

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Source

Identifiers

PMID: 28477304
DOI: 10.1007/s12020-017-1310-9

Genes

MAX
RET
VHL
SDHB
SDHD
SDHA
SDHAF2
SDHC

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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