HMGCS2 Gene 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency NGS Genetic DNA Test
Introduction
The HMGCS2 Gene 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency NGS Genetic DNA Test is a crucial diagnostic tool for identifying metabolic disorders associated with the HMGCS2 gene. This test employs Next-Generation Sequencing (NGS) technology, which allows for comprehensive analysis of genetic material, ensuring precise detection of mutations that may lead to significant health issues.
What the Test Measures
This genetic test measures the presence of mutations in the HMGCS2 gene, which is responsible for producing an enzyme involved in the metabolism of fats and proteins. A deficiency in this enzyme can result in metabolic disorders, leading to serious health complications.
Who Should Consider This Test?
Individuals who exhibit symptoms such as unexplained metabolic issues, neurological symptoms, or have a family history of metabolic disorders should consider this test. Additionally, those at risk due to genetic predisposition may benefit from early detection.
Benefits of Taking the Test
- Early diagnosis of potential metabolic disorders.
- Informed management and treatment options for affected individuals.
- Understanding family risks and implications for relatives.
- Peace of mind through genetic insight.
Understanding Your Results
Results from the HMGCS2 Gene 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency NGS Genetic DNA Test will be provided in a detailed report. It is essential to discuss these results with a healthcare professional for proper interpretation and guidance on the next steps.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| HMGCS2 Gene 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
Don’t wait to understand your genetic health. Book the HMGCS2 Gene 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency NGS Genetic DNA Test today! Call or WhatsApp us at +2348077798758 to schedule your appointment.
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 is required, along with a genetic counselling session to draw a pedigree chart of family members affected with 3-hydroxy-3-methylglutaryl-CoA synthase 2 deficiency.
Specialty: General Physician
Department: Genetics
Method: NGS Technology
Disease Type: Metabolic Disorders
