Serac1 Gene 3-Methylglutaconic Aciduria with Deafness Encephalopathy and Leigh-like Syndrome NGS Genetic DNA Test
The Serac1 Gene 3-Methylglutaconic Aciduria with Deafness Encephalopathy and Leigh-like Syndrome NGS Genetic DNA Test is an advanced diagnostic tool designed to identify specific genetic mutations associated with metabolic disorders. This test utilizes Next Generation Sequencing (NGS) technology to provide precise and comprehensive genetic analysis.
Importance of the Test
This test is particularly important for individuals with a family history of 3-methylglutaconic aciduria, deafness, encephalopathy, and Leigh-like syndrome. Early detection can lead to better management of symptoms and informed decision-making regarding treatment options.
What the Test Measures
The Serac1 Gene test measures genetic alterations that may contribute to the development of metabolic disorders. It specifically targets mutations that can lead to 3-methylglutaconic aciduria and associated conditions.
Who Should Consider This Test
Individuals who should consider this test include:
- Those with symptoms such as unexplained neurological issues, developmental delays, or metabolic disturbances.
- Families with a known history of metabolic disorders, particularly those related to the Serac1 gene.
- Patients seeking genetic counseling for family planning and risk assessment.
Benefits of Taking the Test
- Identifies genetic predispositions to metabolic disorders.
- Informs treatment options and health management strategies.
- Guides family planning decisions through genetic counseling.
- Provides peace of mind for affected families.
Understanding Your Results
Results from the Serac1 Gene test will indicate the presence or absence of specific mutations. A genetic counselor will help interpret the results, providing guidance on potential health implications and next steps.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| Serac1 Gene 3-Methylglutaconic Aciduria with Deafness Encephalopathy and Leigh-like Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To book the Serac1 Gene 3-Methylglutaconic Aciduria with Deafness Encephalopathy and Leigh-like Syndrome NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling and any questions you may have.
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: Clinical history of the patient who is going for the test and a genetic counseling session to draw a pedigree chart of family members affected with the conditions.
Specialty: General Physician | Department: Genetics | Method: NGS Technology | Disease Type: Metabolic Disorders
