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Pheochromocytoma: When to search a germline defect?

Presse medicale (Paris, France : 1983) - 1 Jan 2000

Buffet Alexandre, Burnichon Nelly, Amar Laurence, Gimenez-Roqueplo Anne-Paule

Abstract excerpt

With advances in our understanding of the genetics of pheochromocytomas and paragangliomas (PPGL), the answer to the question 'Should we search for a germline defect in patients diagnosed with PPGL?' has changed considerably since the end of the last century, when PPGL was thought to be inherited in only 10% of cases, because we now know that about 40% of patients carry a germline mutation in one PPGL...

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Identifiers

PMID: 30100270
DOI: 10.1016/j.lpm.2018.07.003

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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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