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VIPAS39 Gene Arthrogryposis Renal Dysfunction and Cholestasis Type 2 Genetic Test

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

-21%

The VIPAS39 Gene Arthrogryposis Renal Dysfunction and Cholestasis Type 2 Genetic Test is a specialized diagnostic examination offered at DNA Labs UAE, designed to detect mutations in the VIPAS39 gene. This gene is crucial for proper cellular function, and mutations within it are associated with a rare disorder known as Arthrogryposis, Renal Dysfunction, and Cholestasis (ARC) syndrome type 2. ARC syndrome is characterized by joint contractures (arthrogryposis), kidney dysfunction (renal dysfunction), and impaired bile flow from the liver (cholestasis), among other symptoms.

The test involves analyzing the patient’s DNA to identify any genetic abnormalities in the VIPAS39 gene that might lead to the condition. It is particularly useful for families with a history of ARC syndrome or for patients presenting symptoms consistent with the disorder, providing crucial information for diagnosis, treatment planning, and genetic counseling.

Conducted at the state-of-the-art facilities of DNA Labs UAE, the test ensures accuracy and reliability. The cost of the test is set at 4400 AED, reflecting the comprehensive nature of the genetic analysis and the specialized expertise required to interpret the results. This test is an essential tool for healthcare providers in diagnosing and managing ARC syndrome, offering hope and direction for affected individuals and their families.

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  • This test is not intended for medical diagnosis or treatment
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VIPAS39 Gene Arthrogryposis Renal Dysfunction and Cholestasis Type 2 Genetic Test

Welcome to DNA Labs UAE, where we offer the VIPAS39 Gene Arthrogryposis Renal Dysfunction and Cholestasis Type 2 Genetic Test. This test is designed to diagnose individuals with a rare genetic disorder called Arthrogryposis, Renal Dysfunction, and Cholestasis type 2 (ARCND2).

Test Details

The VIPAS39 gene is associated with ARCND2, a disorder characterized by joint contractures (arthrogryposis), kidney dysfunction (renal dysfunction), and liver dysfunction (cholestasis). Our NGS (Next-Generation Sequencing) technology allows us to analyze multiple genes simultaneously and identify genetic variations or mutations.

By specifically examining the VIPAS39 gene, we can identify the mutations responsible for causing ARCND2. This information is crucial for diagnosing individuals with the disorder and providing appropriate medical care.

Components and Price

The VIPAS39 Gene Arthrogryposis Renal Dysfunction and Cholestasis Type 2 Genetic Test is priced at 4400.0 AED. The test can be conducted using either blood, extracted DNA, or one drop of blood on an FTA Card.

Report Delivery and Method

After conducting the test, the report will be delivered within 3 to 4 weeks. Our method of analysis, NGS technology, ensures accurate and efficient results.

Test Type and Doctor

The VIPAS39 Gene Arthrogryposis Renal Dysfunction and Cholestasis Type 2 Genetic Test falls under the category of Osteology Dermatology Immunology Disorders. This test is conducted by our experienced dermatologist in our Genetics department.

Pre Test Information

Prior to conducting the VIPAS39 Gene Arthrogryposis Renal Dysfunction and Cholestasis Type 2 Genetic 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 ARCND2.

Conclusion

The VIPAS39 Gene Arthrogryposis Renal Dysfunction and Cholestasis Type 2 Genetic Test is a valuable diagnostic tool for identifying mutations in the VIPAS39 gene associated with ARCND2. This test can be used for diagnosis, carrier testing, prenatal testing, and genetic counseling for families with a history of the disorder. At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services.

Test Name VIPAS39 Gene Arthrogryposis renal dysfunction and cholestasis type 2 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for VIPAS39 Gene Arthrogryposis, renal dysfunction, and cholestasis type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with VIPAS39 Gene Arthrogryposis, renal dysfunction, and cholestasis type 2 NGS Genetic DNA Test gene VIPAS39
Test Details

The VIPAS39 gene is associated with a rare genetic disorder called Arthrogryposis, Renal Dysfunction, and Cholestasis type 2 (ARCND2). This disorder is characterized by joint contractures (arthrogryposis), kidney dysfunction (renal dysfunction), and liver dysfunction (cholestasis).

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify genetic variations or mutations. In the case of ARCND2, NGS genetic testing can be used to identify mutations in the VIPAS39 gene, which is responsible for causing the disorder.

By identifying the specific mutation in the VIPAS39 gene, NGS genetic testing can help in diagnosing individuals with ARCND2. It can also be used for carrier testing, prenatal testing, and genetic counseling for families with a history of ARCND2.

Overall, the VIPAS39 gene Arthrogryposis, renal dysfunction, and cholestasis type 2 NGS genetic test is a diagnostic tool used to identify mutations in the VIPAS39 gene associated with ARCND2.

SKU: TEST-2852 Category:

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