BCS1L Gene Mitochondrial Complex III Deficiency NGS Genetic DNA Test
Introduction to the Test
The BCS1L Gene Mitochondrial Complex III Deficiency NGS Genetic DNA Test is a groundbreaking diagnostic tool designed to detect genetic mutations associated with mitochondrial disorders. Mitochondrial diseases can lead to severe neurological issues, and early detection is crucial for effective management and treatment.
What the Test Measures
This test specifically measures the presence of mutations in the BCS1L gene, which is essential for the proper functioning of the mitochondrial respiratory chain. By using Next-Generation Sequencing (NGS) technology, we can accurately identify any genetic abnormalities that may contribute to mitochondrial dysfunction.
Who Should Consider This Test
Individuals who exhibit symptoms of mitochondrial disorders, such as:
- Neurological deficits
- Muscle weakness
- Seizures
- Developmental delays
- Fatigue and exercise intolerance
Additionally, those with a family history of BCS1L gene mutations or mitochondrial diseases should consider this test, as it can provide valuable information for family planning and management.
Benefits of Taking the Test
- Accurate diagnosis of mitochondrial disorders.
- Guidance for treatment options and management strategies.
- Informed family planning and genetic counseling.
- Peace of mind for patients and their families.
Understanding Your Results
Upon receiving your results, our medical team will provide a comprehensive interpretation. A positive result indicates the presence of a mutation in the BCS1L gene, while a negative result suggests no detectable mutations. It’s essential to discuss your results with a healthcare professional to understand the implications for your health and family.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| BCS1L Gene Mitochondrial Complex III Deficiency NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Sample Type and Turnaround Time
The test requires a sample of blood or extracted DNA, or one drop of blood on an FTA card. The turnaround time for results is approximately 3 to 4 weeks.
Pre-Test Instructions
Prior to taking the test, it is recommended to have a clinical history assessment and a genetic counseling session to create a pedigree chart of family members affected by BCS1L Gene Mitochondrial Complex III deficiency.
Branches and Booking
We have branches across all major cities in Kenya, including Nairobi, Mombasa, and Kisumu. To book the BCS1L Gene Mitochondrial Complex III Deficiency NGS Genetic DNA Test, please call or WhatsApp us at +254711564616. Take the first step towards understanding your health today!
