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Clinical and Genetic Features of Patients With Fanconi Anemia in Lebanon and Report on Novel Mutations in the FANCA and FANCG Genes.

Journal of pediatric hematology/oncology - 1 Jul 2021

Farah Roula A, Nair Pratibha, Koueik Jack, Yammine Tony, Khalifeh Hassan, Korban Rima, Collet Agnes, Khayat Claudia, Dubois-Denghien Catherine, Chouery Eliane, Blanluet Maud, El-Hayek Stephany, Stoppa-Lyonnet Dominique, Megarbane Andre

Abstract excerpt

Fanconi anemia (FA) is the most common inherited bone marrow failure syndrome and presents with cytopenias, characteristic physical features, increased chromosomal breaks, and a higher risk of malignancy. Genetic features of this disease vary among different ethnic groups. We aimed to identify the incidence, outcome, overall condition, and genetic features of patients affected with FA in Lebanon to optimize...

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PMID: 32947577
DOI: 10.1097/MPH.0000000000001909

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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