HSD17B4 Gene Perrault Syndrome NGS Genetic DNA Test
Introduction
The HSD17B4 Gene Perrault Syndrome NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with Perrault syndrome, a condition linked to neurological disorders. This test uses Next Generation Sequencing (NGS) technology to provide comprehensive insights into an individual’s genetic profile, enabling early diagnosis and management of potential health issues.
What the Test Measures
This genetic test specifically measures variations in the HSD17B4 gene, which plays a critical role in the metabolism of steroid hormones. By identifying mutations in this gene, healthcare providers can assess the risk of developing neurological disorders associated with Perrault syndrome.
Who Should Consider This Test?
Individuals with a family history of Perrault syndrome or those displaying symptoms such as hearing loss, ovarian dysfunction, or neurological issues should consider this test. Risk factors include:
- Family history of genetic disorders
- Symptoms of neurological disorders
- Women with unexplained infertility or hearing loss
Benefits of Taking the Test
Taking the HSD17B4 Gene Perrault Syndrome NGS Genetic DNA Test offers numerous benefits, including:
- Early detection of genetic predispositions
- Informed decision-making regarding family planning
- Guidance for personalized treatment options
- Access to genetic counseling for better understanding
Understanding Your Results
Results from the HSD17B4 Gene Perrault Syndrome NGS Genetic DNA Test can provide crucial information about your genetic risks. A genetic counselor will help interpret the results and discuss potential implications for your health and family planning.
Test Pricing
Test Name | Discount Price (NGN) | Regular Price (NGN) |
---|---|---|
HSD17B4 Gene Perrault Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
How to Book the Test
To book the HSD17B4 Gene Perrault Syndrome NGS Genetic DNA Test or for more information, please contact us at +2348110567037. Our team is ready to assist you with any inquiries 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 going for the test is required, along with a genetic counseling session to draw a pedigree chart of affected family members.
This test is conducted under the supervision of qualified neurologists in our Genetics department, ensuring the highest standards of care and accuracy in diagnosis.