APOA1 Gene Amyloidosis Familial Visceral NGS Genetic DNA Test
Introduction to the Test
The APOA1 Gene Amyloidosis Familial Visceral NGS Genetic DNA Test is a specialized diagnostic tool designed to detect genetic mutations associated with familial amyloidosis, a serious metabolic disorder. This test is particularly important for individuals with a family history of amyloidosis, providing valuable insights into their genetic predisposition and enabling early intervention.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) technology to analyze the APOA1 gene. It detects specific mutations that may lead to the production of abnormal proteins, which can accumulate in organs and tissues, causing significant health issues.
Who Should Consider This Test?
Individuals who should consider the APOA1 Gene Amyloidosis test include:
- Those with a family history of amyloidosis.
- Patients experiencing symptoms such as unexplained weight loss, heart issues, or kidney problems.
- Individuals with risk factors like a known genetic mutation in the family.
Benefits of Taking the Test
Taking the APOA1 Gene Amyloidosis test offers numerous benefits:
- Early detection of genetic predispositions to amyloidosis.
- Informed decision-making regarding lifestyle changes and medical interventions.
- Guidance for family planning and genetic counseling.
- Peace of mind through understanding one’s genetic health risks.
Understanding Your Results
Results from the APOA1 Gene Amyloidosis test will indicate whether any genetic mutations are present. A genetic counselor will assist in interpreting these results, discussing their implications, and recommending further actions if necessary.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| APOA1 Gene Amyloidosis Familial Visceral NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the APOA1 Gene Amyloidosis Familial Visceral NGS Genetic DNA Test, contact us at DNA Labs Nigeria. Our dedicated team is ready to assist you with the booking process and answer any questions you may have. Call or WhatsApp us at +2348077798758 today!
Test Details
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-test Instructions: Clinical history of the patient and a genetic counseling session to draw a pedigree chart of affected family members.
- Specialty: General Physician
- Department: Genetics
- Method: NGS Technology
- Disease Type: Metabolic Disorders
