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Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family.

Molecular genetics & genomic medicine - 1 Feb 2022

Wafa Abdulsamad, Ali Belal, Moassass Faten, Kheder Maged, Aljapawe Abdulmunim, Al-Halabi Bassel, Mrasek Kristin, Liehr Thomas, Al-Achkar Walid

Abstract excerpt

BACKGROUND: Familial cases of adult acute myeloid leukemia (AML) with germline-mutated CCAAT/enhancer-binding protein-α (CEBPA) gene are a rare entity classified in World Health Organization (WHO) classification 2016. Most families reported in the literature show an autosomal dominant inheritance pattern consistent with a single-gene mutation. METHODS: Here we studied a Syrian family with four individuals...

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Identifiers

PMID: 35032366
DOI: 10.1002/mgg3.1854
PMCID: PMC8830806

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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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