DMGDH Gene Dimethylglycine Dehydrogenase Deficiency NGS Genetic DNA Test
Introduction to the Test
The DMGDH Gene Dimethylglycine Dehydrogenase Deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to identify genetic mutations associated with Dimethylglycine Dehydrogenase Deficiency, a rare metabolic disorder. This test is vital for individuals who may be at risk of this condition, allowing for early diagnosis and management.
What the Test Measures
This genetic test measures the presence of mutations in the DMGDH gene, which can lead to metabolic dysfunction. By analyzing the genetic code, healthcare providers can determine if an individual has the genetic predisposition for this deficiency.
Who Should Consider This Test?
Individuals exhibiting symptoms such as developmental delays, neurological issues, or unexplained metabolic problems should consider this test. Additionally, those with a family history of metabolic disorders or affected relatives are encouraged to undergo testing.
Benefits of Taking the Test
- Early diagnosis can lead to better management of symptoms.
- Understanding genetic predispositions helps in making informed health decisions.
- Facilitates genetic counseling for affected families.
- Provides peace of mind for individuals at risk.
Understanding Your Results
Results from the DMGDH Gene Dimethylglycine Dehydrogenase Deficiency NGS Genetic DNA Test will be available within 3 to 4 weeks. A genetic counselor will guide you through your results, explaining the implications and next steps based on your findings.
Test Pricing
| Test Name | DMGDH Gene Dimethylglycine Dehydrogenase Deficiency NGS Genetic DNA Test |
|---|---|
| Discount Price | 40,000 KSh |
| Regular Price | 56,000 KSh |
Book Your Test Today!
We have branches across all major cities in Kenya, including Nairobi, Mombasa, and Kisumu. Our home sample collection service is also available for your convenience. For more information or to book your test, please call or WhatsApp us at +254711564616.
Note: A clinical history and a genetic counseling session to draw a pedigree chart of affected family members are required before proceeding with the test.
