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. |
