SLC16A1 Gene Erythrocyte Lactate Transporter Defect NGS Genetic DNA Test
Introduction
The SLC16A1 Gene Erythrocyte Lactate Transporter Defect NGS Genetic DNA Test is an advanced diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to identify mutations in the SLC16A1 gene. This test is essential for understanding metabolic disorders related to lactate transport, which can lead to significant health complications.
What the Test Measures
This genetic test specifically measures the presence of mutations in the SLC16A1 gene, which is responsible for encoding the erythrocyte lactate transporter protein. This protein plays a critical role in the transport of lactate in the body, and defects can result in metabolic dysfunctions.
Who Should Consider This Test
Individuals with a family history of metabolic disorders, unexplained fatigue, or symptoms such as muscle cramps, seizures, or developmental delays should consider this test. Those with a clinical history suggestive of erythrocyte lactate transporter defects are also prime candidates.
Benefits of Taking the Test
- Early identification of genetic predispositions to metabolic disorders.
- Informed decision-making for treatment and management options.
- Guidance for family planning and genetic counseling.
- Improved understanding of personal health risks.
Understanding Your Results
Results from the SLC16A1 Gene Erythrocyte Lactate Transporter Defect NGS Genetic DNA Test will indicate whether mutations are present. A genetic counselor will help interpret these results, providing insights into the implications for health and potential next steps.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 |
| Regular Price | 560,000 |
Booking the Test
To book the SLC16A1 Gene Erythrocyte Lactate Transporter Defect NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with your booking and 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 who is going for the test and a genetic counseling session to draw a pedigree chart of family members affected with erythrocyte lactate transporter defect is required.
For further inquiries, please reach out to our specialists in the Genetics department.
