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GP1BA Gene Bernard Soulier Syndrome Type A1 Genetic Test Cost

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

-21%

The GP1BA Gene Bernard Soulier Syndrome Type A1 Genetic Test is a specialized diagnostic examination available at DNA Labs UAE. Priced at 4400 AED, this test is specifically designed to identify mutations in the GP1BA gene, which are indicative of Bernard-Soulier Syndrome Type A1 (BSS Type A1). BSS Type A1 is a rare inherited blood disorder characterized by a deficiency of glycoprotein Ib, a crucial component of platelet function necessary for normal blood clotting. Individuals with this syndrome often exhibit symptoms such as prolonged bleeding times, easy bruising, and abnormal platelet function.

The test involves collecting a DNA sample from the patient, typically through a blood draw, which is then analyzed in the lab for genetic anomalies associated with the condition. The results from this test can provide essential information for the diagnosis, management, and treatment planning for individuals suspected of having Bernard-Soulier Syndrome Type A1, enabling healthcare providers to offer targeted interventions to mitigate the symptoms and improve the quality of life for affected individuals. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experienced professionals to ensure accurate and reliable test results.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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GP1BA Gene Bernard Soulier syndrome type A1 Genetic Test

Welcome to DNA Labs UAE, where we offer the GP1BA Gene Bernard Soulier syndrome type A1 Genetic Test. This test is designed to diagnose and provide information about the rare inherited bleeding disorder known as Bernard-Soulier syndrome type A1. Read on to learn more about the test and its details.

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

Before undergoing the GP1BA Gene Bernard Soulier syndrome type A1 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the disorder. This will help in analyzing the genetic changes associated with the GP1BA gene.

Test Details

The GP1BA gene is specifically associated with Bernard-Soulier syndrome type A1. Our NGS (Next-Generation Sequencing) genetic testing method is used to analyze the DNA sequence of genes, including GP1BA, to identify any variations or mutations that may be causing the disorder. This type of genetic test is highly accurate and can help confirm a diagnosis of Bernard-Soulier syndrome type A1. It also provides valuable information about the specific genetic changes involved in the disorder.

For more information or to schedule an appointment for the GP1BA Gene Bernard Soulier syndrome type A1 Genetic Test, please contact our Genetics department.

Test Name GP1BA Gene Bernard Soulier syndrome type A1 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 GP1BA Gene Bernard Soulier syndrome type A1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GP1BA Gene Bernard Soulier syndrome type A1 NGS Genetic DNA Test gene GP1BA
Test Details

The GP1BA gene is associated with Bernard-Soulier syndrome type A1, a rare inherited bleeding disorder. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of genes, including GP1BA, to identify any variations or mutations that may be causing the disorder. This type of genetic test can help confirm a diagnosis of Bernard-Soulier syndrome type A1 and provide information about the specific genetic changes involved.