NDUFS1 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test
Introduction
The NDUFS1 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test is a cutting-edge genetic test designed to identify mutations in the NDUFS1 gene, which is crucial for mitochondrial function. Mitochondrial disorders can lead to severe neurological conditions, and early diagnosis is essential for effective management and treatment.
What the Test Measures
This test measures the presence of genetic mutations in the NDUFS1 gene, which can disrupt mitochondrial energy production. By using Next-Generation Sequencing (NGS) technology, we can accurately detect these mutations, providing valuable information for diagnosis.
Who Should Consider This Test
Individuals experiencing symptoms related to mitochondrial dysfunction, such as:
- Unexplained neurological issues
- Muscle weakness
- Developmental delays
- Seizures
- Family history of mitochondrial disorders
should consider this test. Additionally, those with risk factors for genetic conditions should consult their healthcare provider about testing.
Benefits of Taking the Test
- Accurate diagnosis of mitochondrial disorders
- Informed treatment decisions
- Family planning and genetic counseling
- Understanding the risk of passing on genetic conditions
Understanding Your Results
Results will be interpreted by a qualified genetic counselor or medical professional. They will explain the implications of any detected mutations and discuss potential management strategies.
Test Details
| Test Name | Price (NGN) |
|---|---|
| NDUFS1 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test | Discount Price: 400,000 NGN |
| Regular Price: 560,000 NGN |
Booking the Test
To book the NDUFS1 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you in scheduling your appointment and answering any questions you may have.
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 clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with NDUFS1 Gene Mitochondrial Complex I Deficiency are required.
Consult with a neurologist or geneticist to discuss the necessity of this test for your health or that of your family. Early detection can lead to better management of neurological disorders.
