Article
Understanding the Intricacies of Iron Overload Associated With β-Thalassemia: A Comprehensive Review
2023-06-02
Abstract excerpt
β-thalassemia, a congenital genetic hematological disorder characterized by decreased or absence of β-globin chains, leads to decrease in levels of Hemoglobin A. The affected individuals can be categorized into two cohorts based on transfusion dependency: transfusion dependent thalassemia (TDT) and non-transfusion dependent thalassemia (NTDT). Remarkably, despite the primary pathology lying in β-globin chain deple...
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Identifiers and source
- Literature Corpus work
- 0faf5d04-03ea-54c1-96f6-7c2e7749e3c8
- DOI
- 10.20944/preprints202306.0213.v1