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Article

Catecholamine crisis as a first manifestation of familial bilateral pheochromocytoma caused by RET proto-oncogene mutation in codon C 634R.

Endokrynologia Polska - 1 Jan 2015

Zwolak Agnieszka, Rudzki Grzegorz, Świrska Joanna, Dudzińska Marta, Daniluk Jadwiga, Tarach Jerzy

Abstract excerpt

INTRODUCTION: Multiple endocrine neoplasia type 2 (MEN 2) is a genetic disorder caused by mutation in the RET proto-oncogene. MEN 2A includes medullary carcinoma of the thyroid, pheochromocytoma, and primary hyperparathyroidism. The authors present a case study of three family members with bilateral pheochromocytoma in the course of MEN 2A, a catecholamine crisis being the first manifestation of the syndrome in...

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Identifiers

PMID: 26457501
DOI: 10.5603/EP.2015.0056

Genes

RET

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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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