GP1BA Gene von Willebrand Disease Platelet Type Genetic Test sale cost 4400 AED
RUNX1 Gene Platelet Disorder with Associated Myeloid Malignancy Genetic Test sale cost 4400 AED RUNX1 Gene Platelet Disorder with Associated Myeloid Malignancy Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
IGHM Gene Agammaglobulinemia Type 1 Autosomal Recessive Genetic Test sale cost 4400 AED IGHM Gene Agammaglobulinemia Type 1 Autosomal Recessive Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Sale!

GP1BA Gene von Willebrand Disease Platelet Type Genetic Test Cost

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

-21%

The GP1BA Gene von Willebrand Disease Platelet Type Genetic Test is a specialized diagnostic examination designed to detect mutations in the GP1BA gene, which are associated with von Willebrand Disease Platelet Type, also known as Platelet-type von Willebrand disease (PT-VWD). This condition is a rare bleeding disorder that affects the blood’s ability to clot properly, leading to symptoms such as excessive bleeding from minor wounds, easy bruising, and prolonged bleeding after surgery or dental work. The test involves analyzing the patient’s DNA to identify any genetic abnormalities in the GP1BA gene that could lead to this condition.

Conducted at DNA Labs UAE, a leading facility in genetic testing and diagnostics, this test provides critical information for the accurate diagnosis and management of PT-VWD. Understanding the genetic basis of the disease can help healthcare providers tailor treatment strategies to the individual’s specific condition, potentially improving patient outcomes.

The cost of the GP1BA Gene von Willebrand Disease Platelet Type Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the genetic markers associated with the condition. While the price may seem significant, the value of obtaining a precise diagnosis cannot be understated, as it opens the door to targeted treatments and informed healthcare decisions, ultimately enhancing the quality of life for individuals with PT-VWD.

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
Guaranteed Safe Checkout

GP1BA Gene von Willebrand Disease Platelet Type Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab offering the GP1BA Gene von Willebrand Disease Platelet Type Genetic Test. This test helps diagnose von Willebrand disease platelet type (vWD-PT), a rare inherited bleeding disorder. We provide detailed information about the test, including its components, price, sample condition, report delivery time, method, test type, doctor, and test department.

Test Details

The GP1BA gene is associated with von Willebrand disease platelet type (vWD-PT), which is a rare inherited bleeding disorder. vWD-PT is caused by mutations in the GP1BA gene, which encodes the glycoprotein Ib alpha (GPIb) subunit of the von Willebrand factor (VWF) receptor on platelets.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of vWD-PT, NGS genetic testing can be used to identify mutations in the GP1BA gene, allowing for a diagnosis of the disorder.

By analyzing the DNA sequence of the GP1BA gene, NGS can detect specific mutations or variants that are associated with vWD-PT. This information can help healthcare professionals determine the underlying cause of the patient’s bleeding disorder and guide appropriate treatment and management strategies.

It is important to note that NGS genetic testing for vWD-PT is typically performed in specialized laboratories and is usually ordered by a healthcare provider with expertise in bleeding disorders. Genetic counseling is often recommended before and after genetic testing to help individuals understand the implications of the test results and make informed decisions about their healthcare.

Test Name

GP1BA Gene von Willebrand Disease Platelet Type 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

Hematology

Doctor

Hematologist

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for GP1BA Gene von Willebrand Disease Platelet Type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GP1BA Gene von Willebrand Disease Platelet Type NGS Genetic DNA Test gene GP1BA.

Thank you for considering DNA Labs UAE for your genetic testing needs. We strive to provide accurate and reliable results to help you and your healthcare provider make informed decisions about your health. Contact us today to schedule an appointment or for more information about our services.

Test Name GP1BA Gene von Willebrand disease platelet type 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 Hematology
Doctor Hematologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for GP1BA Gene von Willebrand disease platelet type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GP1BA Gene von Willebrand disease platelet type NGS Genetic DNA Test gene GP1BA
Test Details

The GP1BA gene is associated with von Willebrand disease platelet type (vWD-PT), which is a rare inherited bleeding disorder. vWD-PT is caused by mutations in the GP1BA gene, which encodes the glycoprotein Ib alpha (GPIb) subunit of the von Willebrand factor (VWF) receptor on platelets.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of vWD-PT, NGS genetic testing can be used to identify mutations in the GP1BA gene, allowing for a diagnosis of the disorder.

By analyzing the DNA sequence of the GP1BA gene, NGS can detect specific mutations or variants that are associated with vWD-PT. This information can help healthcare professionals determine the underlying cause of the patient’s bleeding disorder and guide appropriate treatment and management strategies.

It is important to note that NGS genetic testing for vWD-PT is typically performed in specialized laboratories and is usually ordered by a healthcare provider with expertise in bleeding disorders. Genetic counseling is often recommended before and after genetic testing to help individuals understand the implications of the test results and make informed decisions about their healthcare.

SKU: TEST-3970 Category:

Related products