Sickle Cell Anemia Trio Prenatal Mutation Detection Test
Introduction
The Sickle Cell Anemia Trio Prenatal Mutation Detection Test is a vital genetic screening tool that helps identify mutations responsible for sickle cell anemia in unborn children. This test is particularly important for expectant parents with a family history of the disease or those belonging to populations with a higher prevalence of sickle cell traits. By detecting these mutations early, parents can make informed decisions about their pregnancy and potential interventions.
What the Test Measures
This test specifically detects mutations in the HBB gene, which is crucial for the production of hemoglobin. The presence of certain mutations can indicate the likelihood of the child inheriting sickle cell anemia or being a carrier of the sickle cell trait.
Who Should Consider This Test?
Expectant parents should consider this test if:
- They have a family history of sickle cell anemia.
- They belong to ethnic groups that are at higher risk of carrying sickle cell mutations.
- They are experiencing symptoms that may indicate a risk of sickle cell disease.
Benefits of Taking the Test
Taking the Sickle Cell Anemia Trio Prenatal Mutation Detection Test offers several benefits:
- Early detection of genetic mutations that could affect the child’s health.
- Informed decision-making regarding pregnancy and potential interventions.
- Peace of mind for expectant parents regarding their child’s health.
Understanding Your Results
Results from the Sickle Cell Anemia Trio Prenatal Mutation Detection Test will provide insight into whether the identified mutations are present. A genetic counselor can help interpret the results and discuss the implications for the pregnancy.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Sickle Cell Anemia Trio Prenatal Mutation Detection Test | 26000 KSh | 36000 KSh |
Sample Requirements
For this test, a sample of 4 mL (2 mL min.) whole blood in a lavender top (EDTA) tube from both parents is required, along with 10 mL (5 mL min.) of amniotic fluid in a sterile screw-capped container. The samples must be shipped refrigerated and must not be frozen. Additionally, a duly filled Prenatal Genetic Testing Consent Form (Form 18) and Genomics Clinical Information Requisition Form (Form 20) are mandatory.
Contact Us
We have branches across Kenya and offer home sample collection services for your convenience. To book the Sickle Cell Anemia Trio Prenatal Mutation Detection Test, please call or WhatsApp us at +254713408028. Ensure your child’s health by taking this essential test today!
