Alfa-talassemia
Trace. Question. Emerge.
Concept
Alpha-thalassemia is a type of thalassemia characterized by mutations in the HBA1 and HBA2 hemoglobin genes, leading to reduced production of alpha-globin chains.
Translations
- ثلاسيميا ألفا ar primary
- α-Thalassämie German primary
- alpha thalassemia English primary
- Alfa talasemia Spanish primary
- thalassémie alpha French primary
- alfa talassemia it primary
- Αサラセミア ja primary
- Alfa-talassemia pt primary
- ⍺型地中海型貧血 zh primary
Etymology
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