NDUFA9 Gene Leigh Syndrome NGS Genetic DNA Test
Introduction to the NDUFA9 Gene Leigh Syndrome NGS Genetic DNA Test
The NDUFA9 Gene Leigh Syndrome NGS Genetic DNA Test is an advanced diagnostic tool designed to identify genetic mutations associated with Leigh syndrome, a severe neurological disorder. This test employs Next Generation Sequencing (NGS) technology to analyze the NDUFA9 gene, which plays a crucial role in mitochondrial function and energy production. Understanding your genetic makeup is essential for managing health risks and making informed decisions.
What the Test Measures
This genetic test specifically measures mutations in the NDUFA9 gene, which can lead to Leigh syndrome and other neurological disorders. By detecting these mutations, healthcare providers can assess the risk of developing these conditions and guide patients toward appropriate management strategies.
Who Should Consider This Test
This test is recommended for individuals who exhibit symptoms of Leigh syndrome, such as:
- Neurological decline
- Developmental delays
- Muscle weakness
- Seizures
Additionally, those with a family history of Leigh syndrome or other mitochondrial disorders should consider this test for proactive health management.
Benefits of Taking the Test
- Identifies genetic predispositions to Leigh syndrome.
- Informs treatment and management options for affected individuals.
- Provides valuable information for family planning and genetic counseling.
- Enhances understanding of neurological disorders and their implications.
Understanding Your Results
After the test, results will be provided along with guidance from healthcare professionals. It is essential to discuss these results with a genetic counselor or neurologist to understand their implications fully. The turnaround time for results is typically 3 to 4 weeks.
Test Pricing
| Price Type | Price (KSh) |
|---|---|
| Discount Price | 40,000 |
| Regular Price | 56,000 |
Sample Collection and Pre-Test Instructions
The sample type required for this test can be blood, extracted DNA, or one drop of blood on an FTA card. It is important to provide a clinical history during the consultation, and a genetic counseling session is recommended to draw a pedigree chart of family members affected by NDUFA9 Gene Leigh syndrome.
Book Your Test Today!
DNA Labs Kenya has branches across all major cities in Kenya, making it easy and convenient to access our services. For more information or to book your NDUFA9 Gene Leigh Syndrome NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
