Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two α-Globin Gene Defects, Hb Taybe D <i>HBA1</i> : C.119_121delCCA Mutation and <i>HBA2</i> : C.*94A

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Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two α-Globin Gene Defects, Hb Taybe D HBA1 : C.119_121delCCA Mutation and HBA2 : C.*94A > G Mutation

Published:2024-03-03 Issue:2 Volume:48 Page:129-132
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Assaf Nada¹²,El Zibaoui Roba³,Monsef Carla¹²,Abi Nassif Tania⁴,Abboud Miguel⁴,Yazbek Soha³

Affiliation:

1. Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Beirut, Lebanon

2. Faculty of Medicine, American University of Beirut, Beirut, Lebanon

3. Department of Biochemistry and Molecular Genetics, Faculty of Medicine, American University of Beirut Medical Center, Beirut, Lebanon

4. Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, American University of Beirut Medical Center, Beirut, Lebanon

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2024.2338850

Reference16 articles.

1. α-thalassaemia

2. Molecular basis of α-thalassemia

3. Incidence of Alpha-Globin Gene Defect in the Lebanese Population: A Pilot Study

4. Knowledge of thalassemia and consanguinity: A multicenter hospital based retrospective cohort study from metropolitan city of Karachi, Pakistan.

5. Alpha-thalassemia

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