SERHL2 Gene Serine Hydrolase Deficiency SERHL2 Related NGS Genetic DNA Test
Introduction
The SERHL2 Gene Serine Hydrolase Deficiency SERHL2 Related NGS Genetic DNA Test is a pivotal diagnostic tool designed to identify mutations associated with serine hydrolase deficiency, a metabolic disorder that can lead to various health complications. Utilizing cutting-edge Next Generation Sequencing (NGS) technology, this test allows for a comprehensive analysis of the SERHL2 gene, providing essential information for patients and healthcare providers.
What the Test Measures
This genetic test detects specific mutations in the SERHL2 gene that are responsible for serine hydrolase deficiency. By analyzing the genetic material, the test can reveal whether an individual carries pathogenic variants that may impact their health and metabolic function.
Who Should Consider This Test?
Individuals with a family history of metabolic disorders, particularly those exhibiting symptoms such as developmental delays, neurological issues, or unexplained metabolic disturbances, should consider this test. Additionally, those with a known family history of SERHL2-related conditions may benefit from early diagnosis and management strategies.
Benefits of Taking the Test
- Early identification of metabolic disorders related to the SERHL2 gene.
- Informed decision-making regarding treatment and management options.
- Ability to provide genetic counseling for family planning.
- Peace of mind through understanding genetic risks.
Understanding Your Results
Results from the SERHL2 Gene Serine Hydrolase Deficiency test will indicate whether pathogenic variants are present. A genetic counselor can assist in interpreting these results, discussing potential implications for health, and advising on next steps based on the findings.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SERHL2 Gene Serine Hydrolase Deficiency NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
Booking the Test
To book the SERHL2 Gene Serine Hydrolase Deficiency SERHL2 Related NGS Genetic DNA Test, please contact us at +2348110567037. Our team is ready to assist you in scheduling your appointment and answering any questions 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 counseling session to draw a pedigree chart of family members affected with serine hydrolase deficiency.
Specialty: General Physician | Department: Genetics | Method: NGS Technology | Disease Type: Metabolic Disorders
