Hemoglobin H disease
| Hemoglobin H disease | |
|---|---|
| Other names | Alpha-thalassemia intermedia |
| Specialty | Hematology |
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]
See also[]
References[]
- ^ "Pathophysiology of alpha thalassemia". www.uptodate.com. Retrieved 2016-08-30.
External links[]
Categories:
- Blood disorders
- Circulatory disease stubs