Sickle Cell Anemia Mutation Detection Test
Introduction
The Sickle Cell Anemia Mutation Detection Test is a crucial diagnostic tool used to identify specific genetic mutations in the HBB gene associated with sickle cell anemia. This test plays a vital role in the early detection and management of sickle cell disease, allowing individuals to make informed health decisions.
What the Test Measures
This test detects mutations in the HBB gene, which are responsible for the production of abnormal hemoglobin that leads to sickle-shaped red blood cells. By identifying these mutations, healthcare providers can assess the risk of developing sickle cell anemia.
Who Should Consider This Test?
Individuals who may consider this test include:
- Those with a family history of sickle cell disease.
- Individuals experiencing symptoms such as severe anemia, pain episodes, or frequent infections.
- People from regions where sickle cell disease is prevalent.
Benefits of Taking the Test
Taking the Sickle Cell Anemia Mutation Detection Test offers several benefits:
- Early detection of sickle cell mutations, allowing for timely intervention.
- Informed family planning and genetic counseling.
- Better management of symptoms and prevention of complications.
Understanding Your Results
Results from the Sickle Cell Anemia Mutation Detection Test will indicate whether specific mutations are present. A positive result means the individual carries the sickle cell trait or has sickle cell disease, while a negative result indicates the absence of these mutations. It is essential to discuss results with a healthcare provider for appropriate guidance and management.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 90,000 NGN |
| Regular Price | 160,000 NGN |
How to Book the Test
To book the Sickle Cell Anemia Mutation Detection Test, please call or WhatsApp us at +2348110567037. Ensure you have a duly filled Genomics Clinical Information Requisition Form (Form 20) ready for submission along with your sample.
Test Details
Turnaround Time: Sample must be submitted by Monday 11 am; report available by Friday.
Sample Type: 4 mL (2 mL min.) whole blood from one Lavender Top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.
Test Components: HBB
Pre-Test Instructions: Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Specialty and Method
This test falls under the specialty of Physicians and Hematologists and is conducted in the Molecular Diagnostics department using PCR and Sequencing methods.
