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Article

MEN2B syndrome - paediatric case report.

Pediatric endocrinology, diabetes, and metabolism - 1 Jan 2020

Zendran Iga, Szlasa Wojciech, Bis Gabriela, Sondaj Katarzyna, Barg Ewa

Abstract excerpt

Multiple endocrine neoplasia 2B (MEN 2B) is a rare syndrome caused by mutation of the RET proto-oncogene. Early-onset medullary thyroid carcinoma (MTC), marfanoid habitus, and mucosal neuromas occur in most cases, and some patients develop pheochromocytoma in later life. We present a case of a 16-year-old girl diagnosed with MEN 2B syndrome with an atypical course of the disease. Our patient had no family history...

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Identifiers

PMID: 33191720
DOI: 10.5114/pedm.2020.97462

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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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