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Article

One genotype with a myriad of phenotypes: A family with multiple endocrine neoplasia.

Endocrine regulations - 1 Jan 2026

Trimeche Oumeyma, Mnif Fatma, Abdelhedi Fatma, Arbi Kaouther El, Lajmi Yosra, Charfi Nadia, Mnif Mouna, Kacem Faten Hadj, Salah Dhouha Ben, Boujelbene Khouloud, Abid Mohammed, Elleuch Mouna, Rekik Nebila

Abstract excerpt

Objective. Multiple endocrine neoplasia type 1 (MEN1) is a very rare genetic disorder characterized by an autosomal dominant inheritance. We aim through this case series to delineate the wide spectrum of its clinical features. Methods. In the present study, we report the clinical and genetic findings of four siblings affected by this disorder. DNA was extracted from patients' blood leukocytes using a...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 41913677
DOI: 10.2478/enr-2026-0004

Genes

MEN1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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