SURF1 Gene Leigh Syndrome Due to COX Deficiency NGS Genetic DNA Test
Introduction
The SURF1 Gene Leigh Syndrome due to COX deficiency NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the SURF1 gene, which can lead to Leigh syndrome, a severe neurological disorder characterized by progressive loss of mental and movement abilities. This test is crucial for patients exhibiting symptoms of Leigh syndrome, allowing for early diagnosis and intervention.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) technology to detect specific genetic mutations associated with Leigh syndrome due to COX deficiency. By analyzing the SURF1 gene, it provides valuable insights into the genetic factors contributing to the disorder.
Who Should Consider This Test?
Individuals who should consider the SURF1 Gene Leigh Syndrome test include:
- Patients showing symptoms of Leigh syndrome such as developmental delays, loss of motor skills, and neurological regression.
- Individuals with a family history of Leigh syndrome or other mitochondrial disorders.
- Those seeking genetic counseling for family planning and understanding hereditary risks.
Benefits of Taking the Test
- Early diagnosis of Leigh syndrome, enabling timely treatment and management.
- Informed family planning decisions through understanding genetic risks.
- Access to tailored medical care and support based on genetic findings.
- Peace of mind for patients and families regarding their genetic health.
Understanding Your Results
Results from the SURF1 Gene Leigh Syndrome test will indicate the presence or absence of mutations in the SURF1 gene. A positive result may confirm the diagnosis of Leigh syndrome, while a negative result can provide reassurance or indicate the need for further testing. It is essential to discuss results with a healthcare provider for proper interpretation and guidance.
Test Name and Price
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SURF1 Gene Leigh Syndrome Due to COX Deficiency NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
Book the Test
To schedule your SURF1 Gene Leigh Syndrome due to COX deficiency NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Don’t wait any longer to understand your genetic health and make informed decisions for your family’s future!
Turnaround Time: 3 to 4 weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-test Instructions: A clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected with SURF1 Gene Leigh syndrome due to COX deficiency.
Specialty: Neurology
Department: Genetics
Method: NGS Technology
Disease Type: Neurological Disorders
