PDHX Gene Lacticacidemia Due To PDX1 Deficiency NGS Genetic DNA Test
Introduction to the Test
The PDHX Gene Lacticacidemia due to PDX1 deficiency NGS Genetic DNA Test is a specialized diagnostic tool designed to identify mutations in the PDHX gene that can lead to metabolic disorders. This test employs Next-Generation Sequencing (NGS) technology to analyze genetic material, providing critical insights into an individual’s health. Understanding the genetic basis of lacticacidemia is vital for effective management and treatment of affected individuals.
What the Test Measures
This test detects mutations in the PDHX gene that are associated with lacticacidemia due to PDX1 deficiency. By identifying these mutations, healthcare providers can better understand the underlying causes of metabolic dysfunction in patients.
Who Should Consider This Test
Individuals who experience symptoms such as unexplained fatigue, recurrent vomiting, and neurological issues may benefit from this test. Additionally, those with a family history of metabolic disorders or lacticacidemia should consider genetic testing to assess their risk.
Benefits of Taking the Test
- Early diagnosis of metabolic disorders.
- Informed treatment decisions based on genetic insights.
- Guidance for family planning and risk assessment for relatives.
- Access to genetic counseling for better understanding and management of the condition.
Understanding Your Results
Results from the PDHX Gene Lacticacidemia due to PDX1 deficiency NGS Genetic DNA Test will be interpreted by qualified geneticists. They will provide a comprehensive report detailing any identified mutations and their implications for health and treatment options. It is important to consult with a healthcare provider to discuss the results and potential next steps.
Test Pricing
| Price Type | Amount (KSh) |
|---|---|
| Discount Price | 40,000 |
| Regular Price | 56,000 |
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required can be blood or extracted DNA, or even one drop of blood on an FTA card. Prior to the test, a clinical history review and a genetic counseling session to draw a pedigree chart of family members affected by lacticacidemia due to PDX1 deficiency are recommended.
Book Your Test Today!
We have branches across Kenya, including Nairobi, Mombasa, and Kisumu. For your convenience, we also offer home sample collection services. Take the first step towards understanding your health by booking the PDHX Gene Lacticacidemia due to PDX1 deficiency NGS Genetic DNA Test today. Call or WhatsApp us at +254711564616.
