SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency NGS Genetic DNA Test
Introduction
The SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency NGS Genetic DNA Test is a critical diagnostic tool designed to identify mutations in the SLC16A1 gene, which plays a vital role in metabolic processes. Understanding these mutations is essential for diagnosing metabolic disorders, providing insights into potential health risks, and guiding treatment options.
What the Test Measures
This genetic test specifically detects mutations in the SLC16A1 gene, which are responsible for Monocarboxylate Transporter 1 deficiency. This deficiency can lead to various metabolic disorders, affecting energy production and utilization in the body.
Who Should Consider This Test
Individuals exhibiting symptoms of metabolic disorders, such as unexplained fatigue, muscle weakness, or developmental delays, should consider the SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency NGS Genetic DNA Test. Family history of metabolic conditions also increases the likelihood of genetic mutations that this test can identify.
Benefits of Taking the Test
- Early identification of genetic mutations allows for timely intervention.
- Informs healthcare providers about potential treatment options.
- Helps in genetic counseling for affected families.
- Supports informed decision-making regarding lifestyle and health management.
Understanding Your Results
Results from the SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency NGS Genetic DNA Test will indicate whether mutations are present. A genetic counseling session is recommended to interpret results accurately, discuss implications, and explore potential management strategies.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Sample Type and Turnaround Time
The test requires a sample of blood or extracted DNA, or one drop of blood on an FTA card. The turnaround time for results is approximately 3 to 4 weeks.
Pre-Test Instructions
Prior to undergoing the SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency NGS Genetic DNA Test, patients should have a clinical history reviewed and may benefit from a genetic counseling session to create a pedigree chart of family members affected by this deficiency.
Book Your Test Today
We have branches across Kenya, making it convenient for you to access our services. To book the SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency NGS Genetic DNA Test, call or WhatsApp us at +254711564616. Don’t wait; take a proactive step towards understanding your health today!
