BCAT1 Gene Branched-Chain Aminotransferase 1 Deficiency NGS Genetic DNA Test
Introduction to the Test
The BCAT1 Gene Branched-Chain Aminotransferase 1 Deficiency NGS Genetic DNA Test is an advanced diagnostic tool designed to identify deficiencies in the branched-chain amino acid metabolism. This test is crucial for detecting metabolic disorders that can significantly impact an individual’s health. By utilizing Next Generation Sequencing (NGS) technology, we can provide precise and reliable results, aiding in timely diagnosis and management of related health conditions.
What the Test Measures
This test specifically measures variations in the BCAT1 gene, which is responsible for encoding the branched-chain aminotransferase enzyme. This enzyme plays a vital role in the metabolism of branched-chain amino acids, and deficiencies can lead to serious metabolic disorders.
Who Should Consider This Test?
Individuals who exhibit symptoms such as:
- Neurological issues
- Developmental delays
- Unexplained metabolic disturbances
Additionally, those with a family history of metabolic disorders should consider this test to assess their risk and ensure appropriate management.
Benefits of Taking the Test
- Early detection of metabolic disorders.
- Informed decision-making regarding treatment options.
- Peace of mind for individuals and families.
- Guidance for dietary and lifestyle adjustments.
Understanding Your Results
Results from the BCAT1 Gene Branched-Chain Aminotransferase 1 Deficiency NGS Genetic DNA Test will be provided within 3 to 4 weeks. It is essential to discuss these results with a healthcare professional who can provide guidance on the implications and potential next steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| BCAT1 Gene Branched-Chain Aminotransferase 1 Deficiency NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Booking Your Test
We have branches across Kenya and offer a convenient home sample collection service. To book your test or for further inquiries, please call or WhatsApp us at +254711564616. Ensure you have a clinical history ready and consider a genetic counselling session to create a family pedigree chart, especially if there are known cases of Branched-chain aminotransferase 1 deficiency in your family.
