ALDH4A1 Gene Hyperprolinemia Type 2 NGS Genetic DNA Test
Introduction
The ALDH4A1 Gene Hyperprolinemia Type 2 NGS Genetic DNA Test is a specialized genetic test that helps in the diagnosis of hyperprolinemia type 2, a metabolic disorder. This condition arises due to mutations in the ALDH4A1 gene, which is responsible for the metabolism of proline, an amino acid. Understanding your genetic predisposition through this test is essential for effective management and treatment of the disorder.
What the Test Measures
This NGS (Next Generation Sequencing) test detects mutations in the ALDH4A1 gene, providing a comprehensive analysis of your genetic makeup. By identifying these mutations, healthcare providers can better understand the risk of developing hyperprolinemia type 2 and related metabolic disorders.
Who Should Consider This Test
Individuals who may benefit from this test include:
- Those exhibiting symptoms of hyperprolinemia, such as neurological issues or developmental delays.
- Individuals with a family history of metabolic disorders.
- Patients referred by a general physician or geneticist for further evaluation of metabolic conditions.
Benefits of Taking the Test
- Early diagnosis of hyperprolinemia type 2 can lead to timely interventions.
- Understanding genetic risks can inform lifestyle and dietary choices.
- Provides valuable information for family planning and genetic counseling.
Understanding Your Results
Results from the ALDH4A1 Gene Hyperprolinemia Type 2 NGS Genetic DNA Test will indicate whether any mutations were detected. A genetic counseling session is recommended to interpret the results accurately and discuss the implications for you and your family.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| ALDH4A1 Gene Hyperprolinemia Type 2 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the ALDH4A1 Gene Hyperprolinemia Type 2 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with any questions and guide you through the booking process.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood
Pre-Test Instructions: A clinical history of the patient going for the test is required, along with a genetic counseling session to draw a pedigree chart of family members affected with hyperprolinemia type 2.
Specialty: General Physician
Department: Genetics
Method: NGS Technology
Disease Type: Metabolic Disorders
