SLC25A20 Gene Carnitine-Acylcarnitine Translocase Deficiency NGS Genetic DNA Test
The SLC25A20 Gene Carnitine-Acylcarnitine Translocase Deficiency NGS Genetic DNA Test is a crucial diagnostic tool designed to identify genetic mutations associated with carnitine-acylcarnitine translocase deficiency. This condition is linked to metabolic disorders that can significantly impact an individual’s health. Early detection through this test can play a vital role in managing potential health complications.
What the Test Measures
This genetic test utilizes Next Generation Sequencing (NGS) technology to detect mutations in the SLC25A20 gene. It measures the ability of the body to transport carnitine, a vital nutrient that plays a key role in energy production and metabolism.
Who Should Consider This Test
Individuals with symptoms such as unexplained muscle weakness, fatigue, or metabolic crises should consider this test. Additionally, those with a family history of metabolic disorders or genetic conditions related to carnitine transport are encouraged to undergo testing. Risk factors may include:
- Family history of metabolic disorders
- Symptoms of energy deficiency
- Newborns showing signs of metabolic crises
Benefits of Taking the Test
- Early diagnosis of metabolic disorders
- Informed management of health conditions
- Guidance for family planning and genetic counseling
- Access to appropriate treatment options
Understanding Your Results
Results from the SLC25A20 Gene Carnitine-Acylcarnitine Translocase Deficiency NGS Genetic DNA Test will provide insights into whether a genetic mutation is present. A genetic counselor will help interpret the results and discuss potential next steps, including treatment options and lifestyle changes.
Test Name and Price
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book Your Test Today!
Don’t wait to take control of your health. Book the SLC25A20 Gene Carnitine-Acylcarnitine Translocase Deficiency NGS Genetic DNA Test today by calling or WhatsApp at +2348077798758. Our dedicated team is here to assist you with any questions and guide you through the booking process.
Turnaround time for results is approximately 3 to 4 weeks, and we accept samples of blood or extracted DNA, or one drop of blood on an FTA card. Ensure to bring your clinical history and consider a genetic counseling session to help draw a pedigree chart of family members affected with Carnitine-acylcarnitine translocase deficiency.
