SERHL2 Gene Serine Hydrolase Deficiency SERHL2 Related NGS Genetic DNA Test
Introduction to the Test
The SERHL2 Gene Serine Hydrolase Deficiency SERHL2 Related NGS Genetic DNA Test is an advanced diagnostic tool designed to identify genetic mutations associated with metabolic disorders. This test employs Next-Generation Sequencing (NGS) technology to analyze the SERHL2 gene, which plays a crucial role in various biochemical processes in the body.
What the Test Measures
This genetic test detects mutations in the SERHL2 gene, which can lead to serine hydrolase deficiency. By analyzing the genetic material, the test can confirm or rule out the presence of genetic variants that may contribute to metabolic disorders.
Who Should Consider This Test
Individuals with a family history of metabolic disorders or those exhibiting symptoms such as unexplained developmental delays, neurological issues, or metabolic imbalances should consider this test. Risk factors include:
- Family history of SERHL2-related conditions
- Symptoms of metabolic disorders
- Previous genetic diagnoses in family members
Benefits of Taking the Test
Taking the SERHL2 Gene Serine Hydrolase Deficiency NGS Genetic DNA Test has several benefits, including:
- Accurate diagnosis of genetic conditions
- Informed decision-making regarding treatment options
- Guidance for family planning and genetic counseling
- Access to tailored healthcare solutions
Understanding Your Results
Results from the SERHL2 Gene test will be provided along with a detailed report explaining the findings. It is essential to consult with a healthcare professional to interpret the results accurately and discuss potential next steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SERHL2 Gene Serine Hydrolase Deficiency NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Booking the Test
We have branches across all major cities in Kenya, making it easy for you to access our services. To book the SERHL2 Gene Serine Hydrolase Deficiency NGS Genetic DNA Test, please call or WhatsApp us at +254711564616. Our team is ready to assist you with your testing needs.
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 genetic counseling session is recommended to draw a pedigree chart of family members affected by serine hydrolase deficiency.
Take the first step towards understanding your genetic health today!
