Thalassemia Alpha Trio Prenatal Mutation Detection Test
Introduction
The Thalassemia Alpha Trio Prenatal Mutation Detection Test is a crucial diagnostic tool designed for expectant parents to identify potential genetic disorders in their unborn child. This test employs advanced techniques such as PCR (Polymerase Chain Reaction) and MLPA (Multiplex Ligation-dependent Probe Amplification) to detect mutations associated with alpha thalassemia, a genetic blood disorder that can lead to serious health complications.
What the Test Measures
This test measures the presence of specific mutations in the alpha globin genes that can result in thalassemia. By analyzing blood samples from both parents and amniotic fluid, the test can accurately assess the risk of the fetus inheriting these genetic conditions.
Who Should Consider This Test
Expectant parents who have a family history of thalassemia or other genetic disorders should consider this test. Symptoms that may indicate a risk include:
- Previous children with thalassemia or related conditions
- Family members diagnosed with genetic blood disorders
- Ethnic background associated with higher thalassemia prevalence (e.g., Mediterranean, African, Asian descent)
Benefits of Taking the Test
Taking the Thalassemia Alpha Trio Prenatal Mutation Detection Test offers several benefits:
- Early detection of potential genetic disorders in the fetus
- Informed decision-making for parents regarding pregnancy management
- Access to specialized care and counseling if a genetic condition is detected
- Peace of mind for expecting parents
Understanding Your Results
Results from the Thalassemia Alpha Trio Prenatal Mutation Detection Test will be provided in a comprehensive report. It is essential to discuss these results with a qualified healthcare provider, who can guide you on the implications and next steps based on the findings.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Thalassemia Alpha Trio Prenatal Mutation Detection Test | 32,000 KSh | 44,000 KSh |
How to Book the Test
We have branches across Kenya, including major cities like Nairobi, Mombasa, and Kisumu. You can also opt for our home sample collection service for your convenience. To book the Thalassemia Alpha Trio Prenatal Mutation Detection Test, please call or WhatsApp us at +254711564616.
Sample Requirements
The test requires:
- 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube from both parents
- 10 mL (5 mL min.) amniotic fluid in a sterile screw-capped container
Duly filled Prenatal Genetic Testing Consent Form (Form 18) & Genomics Clinical Information Requisition Form (Form 20) is mandatory. Samples should be shipped refrigerated and must not be frozen.
Turnaround Time
Sample collection must be done by Monday 9 AM, with results available by Friday.
Ensure the health of your unborn child with the Thalassemia Alpha Trio Prenatal Mutation Detection Test. Book your appointment today!
