LAS1L Gene Wilson-Turner Syndrome NGS Genetic DNA Test
Introduction to the Test
The LAS1L Gene Wilson-Turner Syndrome NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to identify genetic variations associated with Wilson-Turner syndrome. This test plays a crucial role in understanding the genetic basis of neurological disorders, enabling early diagnosis and intervention.
What the Test Measures
This test specifically measures genetic mutations in the LAS1L gene, which have been linked to Wilson-Turner syndrome. By analyzing the DNA, healthcare professionals can determine the presence of these mutations and assess the risk of developing related neurological conditions.
Who Should Consider This Test?
Individuals who may benefit from the LAS1L Gene Wilson-Turner Syndrome NGS Genetic DNA Test include:
- Those with a family history of Wilson-Turner syndrome.
- Patients exhibiting symptoms such as developmental delays, cognitive impairments, or other neurological issues.
- Individuals seeking genetic counseling to understand their risk factors better.
Benefits of Taking the Test
- Early identification of genetic predispositions to neurological disorders.
- Informed decision-making regarding treatment and management options.
- Access to genetic counseling and support for affected families.
- Peace of mind through understanding one’s genetic health.
Understanding Your Results
Results from the LAS1L Gene Wilson-Turner Syndrome NGS Genetic DNA Test will provide insights into the presence or absence of genetic mutations. A genetic counselor will help interpret these results, discussing their implications for health and family planning.
Test Name and Price
| Discount Price | 400,000 NGN |
|---|---|
| Regular Price | 560,000 NGN |
Booking the Test
To book the LAS1L Gene Wilson-Turner Syndrome NGS Genetic DNA Test, please contact us at +2348077798758. Ensure you have a clinical history prepared and consider scheduling a genetic counseling session to discuss your family’s medical history.
Test Details
- 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 and a genetic counseling session to draw a pedigree chart of affected family members.
- Specialty: Neurology
- Department: Genetics
- Method: NGS Technology
- Disease Type: Neurological Disorders
