HOGA1 Gene Hyperoxaluria Type 3 NGS Genetic DNA Test
Introduction to the HOGA1 Gene Hyperoxaluria Type 3 NGS Genetic DNA Test
The HOGA1 Gene Hyperoxaluria Type 3 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with hyperoxaluria type 3, a rare metabolic disorder. This test employs Next Generation Sequencing (NGS) technology to provide accurate and comprehensive results, allowing healthcare providers to make informed decisions regarding patient care.
What the Test Measures
This genetic test specifically measures mutations in the HOGA1 gene, which is crucial for the metabolism of glyoxylate. By detecting these mutations, the test helps determine the risk of developing hyperoxaluria type 3, a condition that can lead to kidney stones and renal failure if left untreated.
Who Should Consider This Test?
Individuals who may benefit from the HOGA1 Gene Hyperoxaluria Type 3 NGS Genetic DNA Test include:
- Patients with a family history of hyperoxaluria type 3 or related metabolic disorders.
- Individuals experiencing recurrent kidney stones or signs of renal impairment.
- Patients seeking genetic counseling for family planning or management of metabolic conditions.
Benefits of Taking the Test
- Early diagnosis can lead to timely interventions, potentially preventing severe complications.
- Understanding genetic predispositions helps in personalized treatment plans.
- Provides valuable information for family members regarding their risk of hereditary conditions.
Understanding Your Results
Results from the HOGA1 Gene Hyperoxaluria Type 3 NGS Genetic DNA Test will be interpreted by qualified genetic counselors. They will explain the significance of any detected mutations, discuss the implications for health, and guide you on the next steps, if necessary.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book Your Test Today!
To book the HOGA1 Gene Hyperoxaluria Type 3 NGS Genetic DNA Test or for more information, please contact us at +2348077798758. Our dedicated team is ready to assist you in understanding your health better.
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 going for the test and a Genetic Counseling session to draw a pedigree chart of family members affected with Hyperoxaluria type 3 is recommended.
Specialty: General Physician | Department: Genetics | Method: NGS Technology | Disease Type: Metabolic Disorders
