GP1BB Gene Bernard Soulier Syndrome Type B Genetic Test sale cost 4400 AED
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GP1BB Gene Bernard Soulier Syndrome Type B Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The GP1BB Gene Bernard Soulier Syndrome Type B Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the GP1BB gene. This gene plays a crucial role in the proper functioning of platelets, which are essential for blood clotting. Mutations in the GP1BB gene can lead to Bernard-Soulier Syndrome Type B, a rare inherited bleeding disorder characterized by abnormally large platelets, a reduced number of platelets, and prolonged bleeding times.

This genetic test involves collecting a DNA sample, typically through a blood draw, and examining the GP1BB gene for specific mutations associated with the syndrome. The process is critical for individuals with a family history of the condition or those exhibiting symptoms suggestive of Bernard-Soulier Syndrome, such as easy bruising, frequent nosebleeds, or excessive bleeding from minor wounds.

At DNA Labs UAE, the GP1BB Gene Bernard Soulier Syndrome Type B Genetic Test is offered at a cost of 4400 AED. The test is conducted in a state-of-the-art laboratory setting by experienced geneticists and laboratory technicians. Results from this test can provide essential information for diagnosis, allowing for appropriate management and treatment strategies to be implemented, and can also offer valuable insights for family planning purposes.

Given the implications of the results, genetic counseling is often recommended alongside the test to help individuals and families understand the potential outcomes and to provide support in making informed decisions about their health and future.

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GP1BB Gene Bernard Soulier syndrome type B Genetic Test

At DNA Labs UAE, we offer the GP1BB Gene Bernard Soulier syndrome type B Genetic Test to help diagnose and manage this rare inherited bleeding disorder. This test analyzes the GP1BB gene for mutations associated with Bernard-Soulier syndrome type B.

Test Details

The GP1BB Gene Bernard-Soulier syndrome type B NGS Genetic Test is a genetic test that utilizes Next-Generation Sequencing (NGS) technology. It allows for the simultaneous analysis of multiple genes, including the GP1BB gene, to identify potential disease-causing mutations.

Bernard-Soulier syndrome type B is characterized by a deficiency or dysfunction of the glycoprotein Ib-IX-V complex on platelets, leading to abnormal platelet function and increased bleeding tendency. This test can be used for diagnostic purposes or for carrier screening in individuals with a family history of the syndrome.

Test Components and Price

The cost of the GP1BB Gene Bernard Soulier syndrome type B Genetic Test is AED 4400.0. The test can be performed using blood samples, extracted DNA, or one drop of blood on an FTA card.

Report Delivery and Turnaround Time

After the sample is collected, the report will be delivered within 3 to 4 weeks.

Test Type and Doctor

The GP1BB Gene Bernard Soulier syndrome type B Genetic Test falls under the category of Vascular Diseases. It is recommended to consult a General Physician for this test.

Test Department and Pre Test Information

The test is conducted by our Genetics department. Prior to the test, it is important to provide the clinical history of the patient who is going for the GP1BB Gene Bernard Soulier syndrome type B NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the syndrome.

Conclusion

The GP1BB Gene Bernard Soulier syndrome type B Genetic Test is a valuable tool for diagnosing and managing this rare bleeding disorder. By analyzing the GP1BB gene, this test can provide important information for affected individuals and their families. If you have a family history of Bernard-Soulier syndrome type B or suspect that you may be affected, we recommend consulting a General Physician and considering this genetic test.

Test Name GP1BB Gene Bernard Soulier syndrome type B Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Vascular Diseases
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for GP1BB Gene Bernard Soulier syndrome type B NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GP1BB Gene Bernard Soulier syndrome type B NGS Genetic DNA Test gene GP1BB
Test Details

GP1BB Gene Bernard-Soulier syndrome type B NGS Genetic Test is a genetic test that analyzes the GP1BB gene for mutations associated with Bernard-Soulier syndrome type B. This syndrome is a rare inherited bleeding disorder characterized by a deficiency or dysfunction of the glycoprotein Ib-IX-V complex on platelets, leading to abnormal platelet function and increased bleeding tendency. The NGS (Next-Generation Sequencing) technique allows for the simultaneous analysis of multiple genes, including the GP1BB gene, to identify potential disease-causing mutations. This test can be used for diagnostic purposes or for carrier screening in individuals with a family history of Bernard-Soulier syndrome type B. The results of the test can help in the management and treatment of affected individuals and their families.

SKU: TEST-3512 Category:

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