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ATP7B Gene Wilson disease Genetic Test Cost

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

-21%

The ATP7B gene Wilson disease genetic test is a diagnostic tool used to identify mutations in the ATP7B gene, which are responsible for Wilson disease, a rare autosomal recessive disorder. This genetic condition leads to excessive accumulation of copper in the body, affecting the liver, brain, and other organs. Early detection through genetic testing is crucial for managing symptoms and preventing severe complications. The test involves analyzing the DNA to look for specific mutations in the ATP7B gene that are known to cause Wilson disease.

Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services, the ATP7B gene test is available for a cost of 4400 AED. This comprehensive test offers individuals and families critical information regarding the genetic predisposition to Wilson disease, enabling timely intervention and appropriate management strategies. By choosing DNA Labs UAE for this test, patients can expect accurate results, professional confidentiality, and guidance on the implications of the test outcomes.

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ATP7B Gene Wilson Disease Genetic Test

Welcome to DNA Labs UAE, a leading genetic laboratory offering a wide range of genetic tests. In this blog post, we will discuss the ATP7B Gene Wilson Disease Genetic Test. This test is designed to detect mutations in the ATP7B gene associated with Wilson disease.

Test Components

The ATP7B Gene Wilson Disease Genetic Test includes the following components:

  • Test Name: ATP7B Gene Wilson Disease Genetic Test
  • 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: Metabolic Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Before undergoing the ATP7B Gene Wilson Disease Genetic Test, it is important to provide the following information:

  • Clinical History of Patient who is going for ATP7B Gene Wilson Disease NGS Genetic DNA Test
  • A Genetic Counselling session to draw a pedigree chart of family members affected with Wilson disease

Test Details

Wilson disease is an autosomal recessive disorder characterized by the accumulation of copper in various tissues, leading to liver and neurological problems. The ATP7B gene Wilson Disease NGS genetic test utilizes next-generation sequencing (NGS) technology to analyze the ATP7B gene for mutations.

The ATP7B gene provides instructions for producing a protein called copper-transporting ATPase 2, which is responsible for transporting copper out of cells. Mutations in this gene can disrupt the normal copper transport process, resulting in the accumulation of copper in tissues.

The ATP7B Gene Wilson Disease NGS genetic test involves obtaining a DNA sample, typically through a blood sample or cheek swab. The DNA is then sequenced using NGS technology to identify any mutations or variants in the ATP7B gene. The results of the test can help confirm a diagnosis of Wilson disease and guide treatment decisions.

Treatment and Counseling

Treatment for Wilson disease often involves medications to remove excess copper from the body and dietary changes to limit copper intake. It is important to note that genetic testing for Wilson disease should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and guidance.

At DNA Labs UAE, we strive to provide accurate and reliable genetic testing services. If you suspect Wilson disease or have a family history of the condition, consult your general physician to determine if the ATP7B Gene Wilson Disease Genetic Test is right for you. Our dedicated team of professionals is here to support you throughout the testing process and provide the necessary guidance for your healthcare decisions.

Test Name ATP7B Gene Wilson disease 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for ATP7B Gene Wilson disease NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Wilson disease
Test Details

ATP7B gene Wilson disease NGS genetic test is a diagnostic test used to detect mutations in the ATP7B gene associated with Wilson disease. Wilson disease is an autosomal recessive disorder characterized by the accumulation of copper in various tissues, leading to liver and neurological problems.

Next-generation sequencing (NGS) is a high-throughput sequencing technology that allows for the rapid and simultaneous sequencing of multiple genes or the entire genome. In the case of Wilson disease, NGS can be used to analyze the ATP7B gene for mutations.

The ATP7B gene provides instructions for producing a protein called copper-transporting ATPase 2, which is involved in transporting copper out of cells. Mutations in this gene can disrupt the normal copper transport process, leading to the accumulation of copper in tissues.

The ATP7B gene Wilson disease NGS genetic test involves obtaining a DNA sample, typically through a blood sample or cheek swab. The DNA is then sequenced using NGS technology to identify any mutations or variants in the ATP7B gene.

The results of the test can help confirm a diagnosis of Wilson disease and guide treatment decisions. Treatment for Wilson disease often involves medications to remove excess copper from the body and dietary changes to limit copper intake.

It is important to note that genetic testing for Wilson disease should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and guidance.

SKU: TEST-2655