Cox15 Gene Leigh Syndrome NGS Genetic DNA Test
Introduction to the Test
The Cox15 Gene Leigh Syndrome NGS Genetic DNA Test is a vital diagnostic tool that helps identify genetic mutations linked to Leigh syndrome, a severe neurological disorder. This test employs next-generation sequencing (NGS) technology to provide comprehensive insights into the genetic basis of the disease, allowing for early diagnosis and management.
What the Test Measures
This test specifically detects mutations in the Cox15 gene, which plays a critical role in mitochondrial function. Identifying these mutations can help explain the underlying cause of Leigh syndrome in affected individuals.
Who Should Consider This Test?
Individuals who exhibit symptoms of Leigh syndrome, such as developmental delays, loss of motor skills, and neurological decline, should consider this test. Additionally, those with a family history of neurological disorders may benefit from genetic testing to understand their risk.
Benefits of Taking the Test
- Early diagnosis of Leigh syndrome can lead to timely interventions.
- Understanding genetic predispositions can inform treatment options.
- Provides clarity for families regarding hereditary risks.
Understanding Your Results
Results from the Cox15 Gene Leigh Syndrome NGS Genetic DNA Test will be provided within 3 to 4 weeks. A genetic counseling session is recommended to help interpret the findings and discuss potential next steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Cox15 Gene Leigh Syndrome NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Branches and Booking
We have branches across all major cities in Kenya, providing easy access to our diagnostic services. Additionally, we offer home sample collection for your convenience. To book the Cox15 Gene Leigh Syndrome NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
Take the first step towards understanding your health today with our comprehensive genetic testing services!
