About this test
Detects deletions and point variants in the alpha-globin genes HBA1 and HBA2, the cause of alpha thalassemia and HbH disease. MLPA finds the common deletions; Sanger sequencing finds point variants.
- Clinical area
- Inherited disorders
- Method
- Sanger + MLPA
- Sample
- EDTA whole blood · Extracted DNA · Dried blood spot
- Report languages
- EN · AR · RU
When to order
Microcytic anaemia with normal iron and HbA2, premarital and carrier screening, or a family history of alpha thalassemia.
Results are reported to the ordering physician and should be interpreted in clinical context.
Request this test
Offer this test to your patients.
Contract pricing and turnaround times are provided on request for laboratories and clinics.
Inherited disorders