NEU1 Gene Neuraminidase Deficiency NGS Genetic DNA Test
The NEU1 Gene Neuraminidase Deficiency NGS Genetic DNA Test is a vital diagnostic tool that helps identify genetic mutations associated with neuraminidase deficiency, a metabolic disorder. This test utilizes Next Generation Sequencing (NGS) technology to provide accurate and comprehensive insights into the genetic health of individuals. Understanding these genetic factors is crucial for early diagnosis and management of potential health issues.
What the Test Measures
This genetic test specifically measures mutations in the NEU1 gene, which is responsible for producing the enzyme neuraminidase. A deficiency in this enzyme can lead to various metabolic disorders, affecting multiple bodily systems.
Who Should Consider This Test?
Individuals who should consider the NEU1 Gene Neuraminidase Deficiency Test include:
- Those with a family history of metabolic disorders.
- Individuals experiencing symptoms such as developmental delays, skeletal abnormalities, or neurological issues.
- Patients referred by general physicians or genetic counselors for further evaluation.
Benefits of Taking the Test
Taking the NEU1 Gene Neuraminidase Deficiency NGS Genetic DNA Test offers numerous benefits:
- Early detection of genetic mutations that may lead to metabolic disorders.
- Informed decision-making regarding treatment and management options.
- Guidance for family planning based on genetic counseling results.
Understanding Your Results
After the test, results will be provided in a clear and comprehensive format. It is essential to discuss these results with a healthcare professional or genetic counselor to understand their implications fully. Knowledge of your genetic status can significantly impact health management and preventive care.
Test Pricing
| Test Name | Regular Price | Discount Price |
|---|---|---|
| NEU1 Gene Neuraminidase Deficiency NGS Genetic DNA Test | 560000 NGN | 400000 NGN |
Book the Test
To book the NEU1 Gene Neuraminidase 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.
Turnaround time for results is approximately 3 to 4 weeks. The sample type required is blood or extracted DNA, or one drop of blood on an FTA card. Prior to the test, a genetic counseling session is recommended to draw a pedigree chart of family members affected with neuraminidase deficiency.
