Fanconi Anemia (FA): A Comprehensive Overview of Genetics, Symptoms, and Disease Progression

Fanconi anemia (FA) is an autosomal recessive disease caused by a biallelic mutation which mainly occurs in proteins involved in the cell cycle, from DNA synthesis to replication and regeneration. The carrier frequency of disease is 1:300 of live births in the general population. The male-to-femal...

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Bibliographic Details

Main Authors:	Shahameen Aqeel, Areeba Aqeel, Fozia Shamshad, Sana Kashif, Shahjabeen Khan
Format:	Artigo
Language:	Inglês
Published:	Liaquat National Hospital and Medical College 2025-08-01
Series:	Journal of Liaquat National Hospital
Subjects:	fanconi anemia (fa) bone marrow chromosomal abnormalities chromosomal translocations pancytopenia thrombocytopenia
Online Access:	https://journals.lnh.edu.pk/jlnh/pdf/196883a8-dbad-4c57-b611-457b8f9cb146.pdf
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