GP9 Gene Bernard Soulier Syndrome Type C Genetic Test sale cost 4400 AED
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GP9 Gene Bernard Soulier Syndrome Type C Genetic Test Cost

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

-21%

The GP9 Gene Bernard Soulier Syndrome Type C Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the GP9 gene associated with Bernard-Soulier Syndrome Type C. This condition is a rare inherited bleeding disorder characterized by the deficiency or malfunction of platelets, leading to prolonged bleeding times. The GP9 gene plays a critical role in the proper formation and function of platelets. Mutations in this gene can disrupt platelet function, resulting in the symptoms associated with Bernard-Soulier Syndrome.

The test is conducted through a blood sample, where DNA is extracted and analyzed for specific genetic alterations in the GP9 gene. This precise genetic testing helps in confirming the diagnosis, allowing for appropriate management and treatment plans tailored to the patient’s specific condition. Furthermore, it can provide valuable information for family planning and genetic counseling for affected families.

The cost of the GP9 Gene Bernard Soulier Syndrome Type C Genetic Test at DNA Labs UAE is 4400 AED. Given the specialized nature of this test and its potential implications for patient care, it represents a crucial investment for individuals exhibiting symptoms suggestive of Bernard-Soulier Syndrome or those with a family history of the condition. Early and accurate diagnosis can significantly impact the quality of life for individuals with this syndrome, enabling better management of symptoms and reducing the risk of complications associated with excessive bleeding.

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GP9 Gene Bernard Soulier Syndrome Type C Genetic Test

At DNA Labs UAE, we offer the GP9 Gene Bernard Soulier Syndrome Type C Genetic Test for AED 4400.0. This test is used to diagnose and identify genetic variations or mutations associated with Bernard-Soulier Syndrome Type C (BSS-C), a rare inherited bleeding disorder characterized by a deficiency or dysfunction of the platelet glycoprotein complex.

Test Details

The GP9 gene encodes the glycoprotein IX (GP9), which is a subunit of the platelet glycoprotein Ib-IX-V complex. Mutations in the GP9 gene can cause BSS-C. To perform the test, we use Next-Generation Sequencing (NGS) technology to analyze multiple genes simultaneously.

Test Components

  • Price: AED 4400.0
  • 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

Prior to the test, it is important to provide the clinical history of the patient who is going for the GP9 Gene Bernard Soulier Syndrome Type C NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the GP9 gene.

Test Procedure

To perform the GP9 Gene Bernard Soulier Syndrome Type C Genetic Test, a blood sample will be obtained from the individual suspected of having the condition. The DNA in the sample will then be extracted and sequenced using NGS technology. The resulting sequence data will be analyzed to identify any genetic variations or mutations in the GP9 gene.

Test Results

The results of the NGS genetic test can help confirm a diagnosis of BSS-C and provide information about the specific mutation(s) present in the GP9 gene. This information can be useful for genetic counseling, family planning, and management of the condition.

It is important to note that NGS genetic testing may not identify all possible mutations in the GP9 gene, as the technology is constantly evolving and new mutations may be discovered in the future. Therefore, it is essential to consult with a healthcare professional or genetic counselor to understand the limitations and implications of the test results.

Test Name GP9 Gene Bernard Soulier syndrome type C 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 GP9 Gene Bernard Soulier syndrome type C NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GP9 Gene Bernard Soulier syndrome type C NGS Genetic DNA Test gene GP9
Test Details

The GP9 gene encodes the glycoprotein IX (GP9), which is a subunit of the platelet glycoprotein Ib-IX-V complex. Mutations in the GP9 gene can cause Bernard-Soulier syndrome type C (BSS-C), which is a rare inherited bleeding disorder characterized by a deficiency or dysfunction of the platelet glycoprotein complex.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously to identify genetic variations or mutations associated with a particular condition. In the case of BSS-C, NGS genetic testing can be performed to identify mutations in the GP9 gene that may be responsible for the disorder.

NGS genetic testing for BSS-C typically involves obtaining a blood sample from the individual suspected of having the condition. The DNA in the sample is then extracted and sequenced using NGS technology. The resulting sequence data is analyzed to identify any genetic variations or mutations in the GP9 gene.

The results of the NGS genetic test can help confirm a diagnosis of BSS-C and provide information about the specific mutation(s) present in the GP9 gene. This information can be useful for genetic counseling, family planning, and management of the condition.

It is important to note that NGS genetic testing may not identify all possible mutations in the GP9 gene, as the technology is constantly evolving, and new mutations may be discovered in the future. Therefore, it is essential to consult with a healthcare professional or genetic counselor to understand the limitations and implications of the test results.

SKU: TEST-3513 Category:

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