ACADS Gene Acyl-CoA Short-Chain Dehydrogenase Deficiency NGS Genetic DNA Test
Introduction
The ACADS Gene Acyl-CoA Short-Chain Dehydrogenase Deficiency NGS Genetic DNA Test is a vital diagnostic tool used to detect genetic mutations associated with metabolic disorders, particularly those affecting fatty acid metabolism. This test utilizes Next Generation Sequencing (NGS) technology, which allows for precise analysis of the ACADS gene, crucial for understanding metabolic functions.
What the Test Measures
The ACADS Gene test specifically measures variations in the ACADS gene that may lead to Acyl-CoA short-chain dehydrogenase deficiency. This deficiency can result in the body’s inability to properly metabolize certain fats, leading to a range of health issues.
Who Should Consider This Test
This test is recommended for individuals exhibiting symptoms such as:
- Unexplained metabolic crises
- Hypoglycemia
- Muscle weakness
- Developmental delays
Additionally, individuals with a family history of metabolic disorders or those at risk due to genetic predispositions should consider this test.
Benefits of Taking the Test
- Early diagnosis of metabolic disorders
- Informed decision-making regarding treatment options
- Genetic counseling can guide family planning
- Understanding of potential health risks for family members
Understanding Your Results
Results from the ACADS Gene test will provide insights into whether any mutations were detected. A genetic counselor can help interpret these results, discuss implications for health, and outline potential next steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| ACADS Gene Acyl-CoA Short-Chain Dehydrogenase Deficiency NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Branches and Booking
We have branches across all major cities in Kenya, and we also offer home sample collection services for your convenience. To book the ACADS Gene Acyl-CoA Short-Chain Dehydrogenase Deficiency NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
Turnaround Time and Sample Type
The turnaround time for this test is approximately 3 to 4 weeks. The sample type required for testing is blood.
Pre-Test Instructions
Prior to testing, it is essential to have a clinical history of the patient and attend a genetic counseling session to create a pedigree chart of family members affected by Acyl-CoA short-chain dehydrogenase deficiency.
For more information and to book your test, contact us today!
