SLC25A20 Gene Carnitine-Acylcarnitine Translocase Deficiency NGS Genetic DNA Test
Introduction
The SLC25A20 Gene Carnitine-Acylcarnitine Translocase Deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool that helps identify mutations in the SLC25A20 gene, which is crucial for the transport of carnitine and acylcarnitines across the mitochondrial membrane. This test is vital for patients suspected of having metabolic disorders, particularly those related to fatty acid oxidation.
What the Test Measures
This genetic test detects specific mutations in the SLC25A20 gene that may lead to carnitine-acylcarnitine translocase deficiency. By analyzing the DNA, healthcare professionals can determine if a patient has this deficiency that disrupts the metabolism of fatty acids.
Who Should Consider This Test
Individuals who should consider the SLC25A20 Gene Carnitine-Acylcarnitine Translocase Deficiency NGS Genetic DNA Test include:
- Patients exhibiting symptoms of carnitine deficiency, such as muscle weakness or hypoglycemia.
- Those with a family history of metabolic disorders.
- Individuals experiencing unexplained fatigue or metabolic irregularities.
Benefits of Taking the Test
The benefits of this test include:
- Accurate diagnosis of metabolic disorders related to the SLC25A20 gene.
- Informed decision-making regarding treatment options.
- Guidance for family planning and understanding hereditary risks.
Understanding Your Results
Results from the SLC25A20 Gene Carnitine-Acylcarnitine Translocase Deficiency NGS Genetic DNA Test will be interpreted by a qualified genetic counselor or physician. They will provide insights into the implications of your results and discuss potential next steps.
Test Pricing
| Discount Price | Regular Price |
|---|---|
| 40,000 KSh | 56,000 KSh |
Booking Your Test
We have branches across Kenya and offer a convenient home sample collection service. To book the SLC25A20 Gene Carnitine-Acylcarnitine Translocase Deficiency NGS Genetic DNA Test, please call or WhatsApp us at +254713408028. Take the first step towards understanding your health today!
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with Carnitine-acylcarnitine translocase deficiency.
For more information about metabolic disorders and genetic testing, visit our website or contact us directly.
