ALDH6A1 Gene Methylmalonate Semialdehyde Dehydrogenase Deficiency NGS Genetic DNA Test
Introduction
The ALDH6A1 Gene Methylmalonate Semialdehyde Dehydrogenase Deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to detect mutations in the ALDH6A1 gene, which is crucial for proper metabolic function. This test employs Next-Generation Sequencing (NGS) technology to provide a comprehensive analysis of genetic variations that may lead to metabolic disorders.
What the Test Measures
This test specifically measures the presence of mutations in the ALDH6A1 gene, which can result in Methylmalonate Semialdehyde Dehydrogenase Deficiency. By identifying these mutations, healthcare providers can better understand a patient’s metabolic health and potential risks.
Who Should Consider This Test
Individuals with a family history of metabolic disorders, especially those showing symptoms such as developmental delays, neurological issues, or metabolic crises, should consider this test. Additionally, individuals with unexplained metabolic disturbances may benefit from this genetic evaluation.
Benefits of Taking the Test
- Early diagnosis of potential metabolic disorders.
- Guidance for personalized treatment and management plans.
- Informed reproductive choices for families with a history of genetic disorders.
- Peace of mind through understanding genetic health risks.
Understanding Your Results
Results from the ALDH6A1 Gene Methylmalonate Semialdehyde Dehydrogenase Deficiency NGS Genetic DNA Test will be communicated by your healthcare provider. They will explain what the findings mean for your health, potential treatment options, and any necessary follow-up actions.
Test Details
Test Name | Price (NGN) |
---|---|
ALDH6A1 Gene Methylmalonate Semialdehyde Dehydrogenase Deficiency NGS Genetic DNA Test | Discount Price: 400,000 NGN |
Regular Price: 560,000 NGN |
Call to Action
Don’t wait to understand your genetic health. Book the ALDH6A1 Gene Methylmalonate Semialdehyde Dehydrogenase Deficiency NGS Genetic DNA Test today! For more information or to schedule your appointment, call or WhatsApp us at +2348077798758.
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 Genetic Counselling session is recommended to draw a pedigree chart of family members affected with Methylmalonate Semialdehyde Dehydrogenase Deficiency.
Specialty: General Physician
Department: Genetics
Method: NGS Technology
Disease Type: Metabolic Disorders