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. |
