GP1BB Gene Bernard Soulier Syndrome Type B NGS Genetic DNA Test
Introduction
The GP1BB Gene Bernard Soulier Syndrome Type B NGS Genetic DNA Test is an advanced diagnostic tool designed to identify genetic mutations associated with Bernard-Soulier syndrome, a rare bleeding disorder. Utilizing Next-Generation Sequencing (NGS) technology, this test provides comprehensive insights into the GP1BB gene, which is crucial for proper platelet function and vascular health.
What the Test Measures
This test specifically measures the presence of mutations in the GP1BB gene. By analyzing the genetic code, it can detect abnormalities that may lead to the development of Bernard-Soulier syndrome, which is characterized by a deficiency in platelet glycoprotein, leading to bleeding complications.
Who Should Consider This Test?
Individuals who may benefit from this test include:
- Those with a family history of bleeding disorders.
- Patients experiencing unexplained bleeding or bruising.
- Individuals with a clinical diagnosis of Bernard-Soulier syndrome.
- Those undergoing genetic counseling for family planning.
Benefits of Taking the Test
Taking the GP1BB Gene Bernard Soulier Syndrome Type B NGS Genetic DNA Test offers several advantages:
- Early diagnosis of potential genetic disorders.
- Informed decision-making for treatment options.
- Guidance for family planning and risk assessment.
- Access to specialized care and management strategies.
Understanding Your Results
Results from the GP1BB Gene test will be provided in a detailed report, which will include:
- Identification of any genetic mutations.
- Implications of the findings for your health.
- Recommendations for further testing or treatment options.
It is essential to discuss your results with a healthcare professional who can guide you through the implications and next steps.
Test Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| GP1BB Gene Bernard Soulier Syndrome Type B NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the GP1BB Gene Bernard Soulier Syndrome Type B NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling and 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 by the GP1BB gene.
Consult with a general physician or a genetic specialist to understand the importance of this test and how it can benefit your health.
