SUCLG1 Gene Mitochondrial DNA Depletion Syndrome Encephalomyopathic Type with Methylmalonic Aciduria NGS Genetic DNA Test
Introduction to the Test
The SUCLG1 Gene Mitochondrial DNA Depletion Syndrome Encephalomyopathic Type with Methylmalonic Aciduria NGS Genetic DNA Test is a vital diagnostic tool for identifying genetic mutations associated with mitochondrial disorders. This test utilizes Next-Generation Sequencing (NGS) technology to analyze the SUCLG1 gene, which plays a crucial role in mitochondrial function. Understanding these genetic factors is essential for patients presenting symptoms of neurological disorders.
What the Test Measures
This test detects mutations in the SUCLG1 gene, which can lead to mitochondrial DNA depletion syndrome. By identifying these mutations, healthcare providers can better understand the underlying causes of neurological symptoms and tailor treatment plans accordingly.
Who Should Consider This Test
Patients who exhibit symptoms such as:
- Neurological impairments
- Developmental delays
- Muscle weakness
- Seizures
- Fatigue
are encouraged to consider this test. Additionally, individuals with a family history of mitochondrial disorders or unexplained neurological symptoms should consult their healthcare provider about the potential benefits of this test.
Benefits of Taking the Test
- Accurate diagnosis of mitochondrial disorders
- Informed treatment decisions based on genetic insights
- Potential for early intervention and improved patient outcomes
- Understanding hereditary patterns in families
- Access to genetic counseling services for affected families
Understanding Your Results
Results from the SUCLG1 Gene Mitochondrial DNA Depletion Syndrome Test will provide insights into the presence of any mutations. A genetic counselor will help interpret these results, explaining their implications for treatment and family planning.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To schedule your SUCLG1 Gene Mitochondrial DNA Depletion Syndrome Encephalomyopathic Type with Methylmalonic Aciduria NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website to book online. Don’t wait for answers—take the first step towards understanding your health today!
Test Details
- Turnaround Time: 3 to 4 weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-test Instructions: Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with SUCLG1 Gene Mitochondrial DNA depletion syndrome.
For more information, please reach out to our team of specialists in the Genetics department.
