Thalassemia Beta Complete Gene Analysis with MCC Test
Introduction
The Thalassemia Beta Complete Gene Analysis with MCC Test is an advanced diagnostic procedure designed to identify mutations in the HBB gene associated with beta-thalassemia. This test is essential for individuals with a family history of thalassemia or those experiencing symptoms related to this genetic disorder. Understanding your genetic predisposition can significantly impact your health management and family planning.
What the Test Measures
This test specifically measures mutations in the HBB gene, which encodes the beta-globin subunit of hemoglobin. By analyzing these genetic components, the test can detect various forms of beta-thalassemia, enabling healthcare providers to offer targeted treatment options.
Who Should Consider This Test
Individuals who should consider the Thalassemia Beta Complete Gene Analysis with MCC Test include:
- Those with a family history of thalassemia or related genetic disorders.
- Individuals experiencing symptoms such as fatigue, weakness, or anemia.
- Pregnant women with a risk of passing genetic disorders to their offspring.
Benefits of Taking the Test
Taking the Thalassemia Beta Complete Gene Analysis with MCC Test offers several benefits, including:
- Early detection of beta-thalassemia, allowing for timely intervention.
- Informed family planning decisions for couples with a genetic predisposition.
- Personalized treatment options based on genetic findings.
Understanding Your Results
Results from the Thalassemia Beta Complete Gene Analysis with MCC Test will provide insight into the presence of specific mutations. It is crucial to discuss these results with a healthcare provider to understand their implications fully. Your provider can guide you on the next steps based on your results.
Test Name and Price
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Thalassemia Beta Complete Gene Analysis with MCC Test | 42,000 KSh | 56,000 KSh |
Sample Requirements and Instructions
To perform this test, the following sample types are required:
- 3 mL (2 mL min.) whole blood (Maternal) in 1 Lavender top (EDTA) tube.
- 10 mL (5 mL min.) Amniotic fluid / CVS in a sterile screw-capped container.
Samples should 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) is mandatory.
Branches and Booking
We have branches across all major cities in Kenya, making it easy for you to access our services. To book the Thalassemia Beta Complete Gene Analysis with MCC Test or for any inquiries, please call or WhatsApp us at +254711564616. Take the first step towards understanding your genetic health today!
Turnaround Time: Sample must be submitted by 9 AM daily; report available in 21 working days.
Specialty: Hematology
Department: Molecular Diagnostics
Method: Next Generation Sequencing, Fragment Analysis
Disease Type: Genetic Disorders
