Sickle cell anemia
Analysis ID 147
Analysis location “GENESIS” Centre for Medical Genetics
Diagnosed illness Sickle cell anemia
OMIM #603903
Clinical information Sickle cell anemia – autosomal recessive disorder characterized by abnormal shape of erythrocytes due to altered physicochemical properties of hemoglobin. The disease is caused by mutations in the beta hemoglobin chain gene (HBB).
Type of analysis Molecular
Type of biological material 5 ml peripheral blood collected in the EDTA tube
Analyzed genes HBB
Analysis description Sequencing analysis of the HBB gene
Analysis indication Sickle cell anemia
Analysis time 3-4 weeks
Refund Yes
CGM laboratory name Laboratory for Molecular Genetics