SICKLE CELL TRIO PRENATAL MUTATION DETECTION
Sickle Cell Anemia is a multisystem disease associated with episodes of acute illness and progressive organ damage. Hemoglobin polymerization, leading to erythrocyte rigidity and vaso-occlusion, is central to the pathophysiology of the disease, but the importance of chronic anemia, hemolysis, and vasculopathy has been established. The most common cause of sickle cell anemia is the HbS variant. This test is useful for detection of mutations in the HBB gene linked to Sickle cell anemia. This assay check for maternal cell contamination in amniotic fluid.
Parameter(s) covered : 3
Report Frequency: Sample Mon by 11 am; Report Fri
Special Instruction: Duly filled Form G, Prenatal Genetic testing Consent Form (Form 18) and Physician prescription is mandatory. Samples shall be accepted only from registered genetics clinics under PCPNDT Act.
Price : ₹ 10000.00
Parameters
- Amniotic Fluid
- Husband
- Wife