Varied clinical presentation of compound heterozygous thalassemia with delta beta or hereditary persistence of foetal hemoglobin

Varied clinical presentation of compound heterozygous thalassemia with delta beta or hereditary persistence of foetal hemoglobin

Introduction: Delta-beta thalassemia and hereditary persistence of fetal hemoglobin (HPFH) results from a deletion in both the delta and beta genes on chromosome 11. Heterozygous/Homozygous delta-beta thalassemia and HPFH have a varied clinical features including age of presentation, transfusion req...

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Bibliographic Details
Main Authors: Sneha Waghela, Sujata Sharma, Nikita Shah, Harshada Uchil, Radha Ghildiyal
Format: Article
Language:English
Published: Elsevier 2023-03-01
Series:Pediatric Hematology Oncology Journal
Subjects:
Delta beta thalassemia
Hereditary persistent fetal hemoglobin
Non transfusion dependent thalassemia
Anemia
Online Access:http://www.sciencedirect.com/science/article/pii/S2468124523000025

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http://www.sciencedirect.com/science/article/pii/S2468124523000025

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