Beta-Thalassemia/Hb E

Last Updated: August 16 2022

Hemoglobin E beta-thalassemia is a rare blood disease where an individual inherits the hemoglobin E (HbE) gene from one parent and a gene for beta-thalassemia from another. This disease causes growth retardation, spleen enlargement, and cardiovascular complications.

Beta-Thalassemia/Hb E falls under theCardiovascular Healthcategory.

Examine Database: Beta-Thalassemia/Hb E
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