Hemoglobin H disease
Hemoglobin H disease is a type of alpha thalassemia caused by impaired production of three of the four alpha globins, coded by genes HBA1 and HBA2.[1]
| Hemoglobin H disease | |
|---|---|
| Other names | Alpha-thalassemia intermedia |
| Specialty | Hematology |
See also
References
- "Pathophysiology of alpha thalassemia". www.uptodate.com. Retrieved 2016-08-30.
External links
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