GPD1 Gene Hypertriglyceridemia Transient Infantile NGS Genetic DNA Test
Introduction
The GPD1 Gene Hypertriglyceridemia Transient Infantile NGS Genetic DNA Test is an advanced diagnostic tool designed to identify genetic predispositions to hypertriglyceridemia in infants. This test is essential for understanding the underlying genetic factors that contribute to elevated triglyceride levels, which can lead to severe health complications if left unmanaged. By utilizing Next Generation Sequencing (NGS) technology, this test provides precise and comprehensive insights into the GPD1 gene, which plays a significant role in lipid metabolism.
What the Test Measures
This genetic test specifically measures variations in the GPD1 gene that may be linked to transient infantile hypertriglyceridemia. Elevated triglyceride levels in infants can lead to various complications, including pancreatitis and other metabolic disorders. Early detection through this test allows for timely intervention and management.
Who Should Consider This Test?
The GPD1 Gene Hypertriglyceridemia test is recommended for:
- Infants displaying symptoms of hypertriglyceridemia such as abdominal pain, nausea, or unexplained lethargy.
- Families with a history of hyperlipidemia or related metabolic disorders.
- Patients undergoing genetic counseling for familial hypertriglyceridemia.
Benefits of Taking the Test
- Early identification of genetic predispositions to hypertriglyceridemia.
- Guidance for tailored treatment plans to manage triglyceride levels effectively.
- Informed decision-making for families regarding lifestyle and dietary modifications.
- Peace of mind through understanding the genetic factors affecting your child’s health.
Understanding Your Results
Results from the GPD1 Gene Hypertriglyceridemia test will provide insights into the presence of genetic variations associated with hypertriglyceridemia. A genetic counselor will help interpret the results, discussing potential implications for health and necessary follow-up actions.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| GPD1 Gene Hypertriglyceridemia Transient Infantile NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To schedule your GPD1 Gene Hypertriglyceridemia Transient Infantile NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with the booking process and answer any questions you may have regarding the test.
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 by GPD1 Gene Hypertriglyceridemia.
This test falls under the specialty of General Physician and the department of Genetics, focusing on Hepatology, Nephrology, and Endocrinology Disorders.
