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Article

Fanconi Anemia in Mexican Patients: Molecular Spectrum and Clinical Manifestations in a Case Series.

International journal of molecular sciences - 30 Apr 2026

Flores-Leura Fernando Alexis, Brukman-Jiménez Sinhue Alejandro, Corona-Rivera Alfredo, Cuero-Quezada Idalid, Pérez-Becerra José de Jesús, Ramírez-Corona Juan Antonio, Rodríguez-Machuca Víctor Ulises, Ortiz-Sandoval María Magdalena, Hinojosa-Piña Fátima Jazmín, Navarro-Barba Olga Lidia, Corona-Rivera Jorge Román, Bobadilla-Morales Lucina

Abstract excerpt

Fanconi anemia (FA) is a rare inherited disorder characterized by genomic instability, congenital anomalies, and progressive bone marrow failure; such manifestations may vary across populations, partly due to differences in genetic background. This study aims to describe the clinical and molecular spectrum of FA in Mexican patients. A total of 14 patients with clinical suspicion of FA were evaluated; cytogenetic...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 42123592
DOI: 10.3390/ijms27094015
PMCID: PMC13163283

Genes

FANCA
FANCC
FANCE

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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