Back اعتلال الهيموغلوبين Arabic Hemoglobinopatia Catalan Hämoglobinopathie German Hemoglobinopatía Spanish هموگلوبینوپاتی Persian Hémoglobinopathie French Emoglobinopatia Italian 혈색소병증 Korean Hemoglobinopathie Dutch Hemoglobinopatia Polish
| Hemoglobinopathy | |
|---|---|
| Other names | Hemoglobinopathies |
 | |
| Red blood cells from a person with sickle cell trait | |
| Specialty | Hematology  |
Hemoglobinopathy is the medical term for a group of inherited blood disorders involving the hemoglobin, the protein of red blood cells.[1] They are generally single-gene disorders and, in most cases, they are inherited as autosomal recessive traits.[2][3]
There are two main groups: abnormal structural hemoglobin variants caused by mutations in the hemoglobin genes, and the thalassemias, which are caused by an underproduction of otherwise normal hemoglobin molecules. The main structural hemoglobin variants are HbS, HbE and HbC. The main types of thalassemia are alpha-thalassemia and beta thalassemia.[4][2]
- ^ CDC (2019-02-08). "Hemoglobinopathies Research". Centers for Disease Control and Prevention. Retrieved 2019-05-05.
- ^ a b Weatherall, D. J.; Clegg, J. B. (2001). "Inherited haemoglobin disorders: An increasing global health problem". Bulletin of the World Health Organization. 79 (8): 704–712. PMC 2566499. PMID 11545326.
- ^ Shakeel, Hassan (25 March 2023). "Thalassaemia — Knowledge Hub". Genomics Education Programme and NHS England. Retrieved 2025-01-01.
- ^ "Hemoglobinopathies and Thalassemia". medicalassistantonlineprograms.org/. Archived from the original on 2015-01-09. Retrieved 2013-11-07.