SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency NGS Genetic DNA Test
Introduction
The SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency NGS Genetic DNA Test is a crucial diagnostic tool for identifying metabolic disorders linked to the SLC16A1 gene. This genetic test utilizes Next-Generation Sequencing (NGS) technology to analyze the DNA, providing insights into genetic mutations that may lead to serious health implications.
What the Test Measures
This test specifically measures mutations in the SLC16A1 gene, which is responsible for encoding the Monocarboxylate Transporter 1 (MCT1). Deficiencies in this transporter can lead to various metabolic disorders, impacting the body’s ability to transport lactate and other monocarboxylates effectively.
Who Should Consider This Test
Individuals experiencing symptoms such as unexplained fatigue, muscle weakness, or metabolic disturbances should consider this test. Additionally, those with a family history of metabolic disorders or genetic predispositions are encouraged to seek this testing for a thorough understanding of their health risks.
Benefits of Taking the Test
- Early diagnosis of metabolic disorders can lead to timely interventions.
- Understanding genetic predispositions helps in personalized healthcare management.
- Provides valuable information for family planning and genetic counseling.
Understanding Your Results
Results from the SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency Test will indicate the presence or absence of mutations in the SLC16A1 gene. A genetic counselor will assist in interpreting these results, discussing potential health implications, and recommending further actions if necessary.
Test Name and Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
To book the SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Ensure you take the first step towards understanding your health and managing potential genetic risks.
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 counseling session is recommended to draw a pedigree chart of family members affected by Monocarboxylate Transporter 1 deficiency.
This test falls under the specialty of General Physician and the department of Genetics, focusing on metabolic disorders through advanced NGS technology.
