GPD1 Gene Hypertriglyceridemia Transient Infantile NGS Genetic DNA Test
Introduction
The GPD1 Gene Hypertriglyceridemia Transient Infantile NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the GPD1 gene that may lead to hypertriglyceridemia in infants. This condition can result in serious health issues, including metabolic disorders. Early diagnosis through genetic testing is crucial for effective management and intervention.
What the Test Measures
This test detects specific mutations in the GPD1 gene associated with transient infantile hypertriglyceridemia. By analyzing the genetic material, the test provides insights into the likelihood of developing related metabolic disorders.
Who Should Consider This Test
Parents and guardians of infants exhibiting symptoms such as:
- Elevated triglyceride levels
- Unexplained metabolic disturbances
- Family history of metabolic disorders
Individuals at risk due to family history or presenting with symptoms should consider this test for early diagnosis and management.
Benefits of Taking the Test
- Early identification of genetic predispositions.
- Informed decision-making regarding dietary and medical interventions.
- Guidance for potential future health issues.
- Support for family planning through genetic counseling.
Understanding Your Results
Results from the GPD1 Gene Hypertriglyceridemia test will be provided in a detailed report. It is essential to discuss these results with a qualified healthcare provider to understand their implications and the next steps for management.
Test Information and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| GPD1 Gene Hypertriglyceridemia Transient Infantile NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Booking the Test
We have branches across all major cities in Kenya, including Nairobi, Mombasa, and Kisumu, and offer home sample collection services. To book the GPD1 Gene Hypertriglyceridemia Transient Infantile NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected with GPD1 Gene Hypertriglyceridemia.
For more information on genetic testing and our services, feel free to contact us.
