NDUFA12 Gene Leigh Syndrome Due to Mitochondrial Complex I Deficiency NGS Genetic DNA Test
Introduction
The NDUFA12 Gene Leigh Syndrome due to Mitochondrial Complex I Deficiency NGS Genetic DNA Test is an advanced diagnostic tool designed to identify mutations in the NDUFA12 gene, which are linked to Leigh syndrome, a severe neurological disorder. This test is essential for individuals experiencing unexplained neurological symptoms, providing critical insights into their genetic makeup and potential health risks.
What the Test Measures
This genetic test specifically detects mutations associated with mitochondrial complex I deficiency, which can lead to a range of neurological disorders, including Leigh syndrome. By analyzing the NDUFA12 gene, the test helps in understanding the underlying causes of symptoms that may affect the central nervous system.
Who Should Consider This Test
Individuals who may benefit from the NDUFA12 Gene test include:
- Those with developmental delays or neurological decline.
- Patients experiencing unexplained seizures or other neurological symptoms.
- Families with a history of Leigh syndrome or mitochondrial disorders.
Benefits of Taking the Test
Taking the NDUFA12 Gene Leigh Syndrome NGS Genetic DNA Test offers several benefits:
- Accurate identification of genetic mutations.
- Informed family planning and management of potential health risks.
- Guidance for tailored therapeutic interventions.
- Peace of mind for individuals and families regarding genetic predispositions.
Understanding Your Results
Results from the NDUFA12 Gene test will indicate whether mutations are present in the NDUFA12 gene. A healthcare provider will help interpret the results, discussing potential implications for health and family planning. It is crucial to understand that a positive result indicates a genetic predisposition, not a definitive diagnosis of Leigh syndrome.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 |
| Regular Price | 560,000 |
Book the Test
To take control of your health and gain valuable insights into your genetic risks, book the NDUFA12 Gene Leigh Syndrome due to Mitochondrial Complex I Deficiency NGS Genetic DNA Test today! Call or WhatsApp us at +2348077798758 to schedule your appointment.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-test Instructions: A genetic counselling session is recommended to draw a pedigree chart of family members affected with NDUFA12 Gene Leigh syndrome due to mitochondrial complex I deficiency.
Consult with a neurologist or genetic specialist to determine if this test is right for you.
