Unveiling the molecular and comorbidity profile among transfusion-dependent and nontransfusion-dependent beta-thalassemic patients in Baghdad city

BACKGROUND: Beta-thalassemia (BT) is the most common hereditary hemolytic disease in Iraq. The high prevalence rate of this disorder, coupled with, frequently encountered severe clinical course, as well as the life-long burden of comorbidities and complications, have all contributed to its status as...

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Bibliographic Details

Published in:	Iraqi Journal of Hematology
Main Authors:	Atyab Abdulhameed Alaqidi, Hind Shaker Al-Mamoori
Format:	Article
Language:	English
Published:	Wolters Kluwer Medknow Publications 2024-12-01
Subjects:	genotypes hbb gene hybridization nontransfusion dependent transfusion dependent beta-thalassemia
Online Access:	https://journals.lww.com/10.4103/ijh.ijh_27_24