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.
Last Updated: August 16 2022
What works and what doesn't?
Unlock the full potential of Examine