DMGDH Gene Dimethylglycine Dehydrogenase Deficiency NGS Genetic DNA Test
Introduction to the DMGDH Gene Test
The DMGDH Gene Dimethylglycine Dehydrogenase Deficiency NGS Genetic DNA Test is an advanced diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to detect mutations in the DMGDH gene. This gene is critical for the metabolism of dimethylglycine, and deficiencies can lead to severe metabolic disorders. Understanding your genetic predisposition is essential for early intervention and management of potential health issues.
What the Test Measures
This genetic test measures the presence of mutations in the DMGDH gene that may lead to dimethylglycine dehydrogenase deficiency. By analyzing the DNA sample, the test can identify specific genetic variations that contribute to metabolic dysfunction.
Who Should Consider This Test?
Individuals who exhibit symptoms of metabolic disorders, such as developmental delays, neurological problems, or unexplained fatigue, should consider this test. Additionally, those with a family history of metabolic disorders or genetic conditions may benefit from testing to determine their risk.
Benefits of Taking the Test
- Early detection of potential metabolic disorders.
- Informed decision-making regarding treatment options.
- Understanding genetic risks for family planning.
- Access to tailored management strategies based on genetic findings.
Understanding Your Results
After the test is completed, results will be provided to you along with guidance on interpretation. It is crucial to discuss these results with a healthcare professional who can help you understand their implications for your health and any necessary next steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| DMGDH Gene Dimethylglycine Dehydrogenase Deficiency NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
To book the DMGDH Gene Dimethylglycine Dehydrogenase Deficiency NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling and any inquiries you may have.
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 counselling session to draw a pedigree chart of family members affected with dimethylglycine dehydrogenase deficiency.
This test falls under the specialty of General Physician and the department of Genetics, focusing on metabolic disorders through NGS technology.
