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ADA2 Gene Sneddon Syndrome Genetic Test

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

-21%

The ADA2 Gene Sneddon Syndrome Genetic Test is a sophisticated diagnostic tool designed to detect mutations in the ADA2 gene, which are associated with Sneddon Syndrome. Sneddon Syndrome is a rare, progressive disorder characterized by the combination of cerebrovascular disease with livedo reticularis (a mottled discoloration of the skin). This condition can lead to a range of symptoms from skin abnormalities to more severe complications such as strokes or other neurological issues.

The test is conducted at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the test is 4400 AED, reflecting the advanced technology and expertise required to accurately identify the genetic variations linked to this condition. Through a blood sample, the test looks for specific mutations in the ADA2 gene that have been implicated in Sneddon Syndrome. Identifying these mutations can be crucial for the diagnosis, management, and understanding of the disease progression in affected individuals. It also provides valuable information for family planning and the assessment of risk in family members.

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  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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ADA2 Gene Sneddon Syndrome Genetic Test

At DNA Labs UAE, we offer the ADA2 Gene Sneddon syndrome genetic test for individuals who suspect they may have this rare genetic disorder. This test can help diagnose Sneddon syndrome and provide important information for treatment and management.

Test Components

  • Test Name: ADA2 Gene Sneddon syndrome Genetic Test
  • Price: 4400.0 AED
  • Sample Condition: Blood
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Vascular Diseases
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the ADA2 Gene Sneddon syndrome genetic test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the ADA2 Gene Sneddon syndrome NGS Genetic DNA Test gene ADA2.

Test Details

The ADA2 gene is associated with Sneddon syndrome, a rare genetic disorder characterized by the development of skin lesions and neurological symptoms, such as strokes, migraines, and cognitive impairment. Our NGS (Next-Generation Sequencing) genetic testing method allows for the simultaneous analysis of multiple genes, including the ADA2 gene.

NGS genetic testing utilizes advanced sequencing technology to identify genetic variations or mutations that may be linked to Sneddon syndrome. In the context of Sneddon syndrome, the ADA2 gene is sequenced in its entirety to detect any variations or mutations that may be present.

It is crucial to note that genetic testing for Sneddon syndrome and other genetic disorders should be conducted by qualified healthcare professionals or genetic counselors. These experts can interpret the test results and provide appropriate guidance and support for diagnosis, treatment, and management.

Test Name ADA2 Gene Sneddon syndrome Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood
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 ADA2 Gene Sneddon syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ADA2 Gene Sneddon syndrome NGS Genetic DNA Test gene ADA2
Test Details

The ADA2 gene is associated with a rare genetic disorder called Sneddon syndrome. This syndrome is characterized by the development of skin lesions and neurological symptoms, such as strokes, migraines, and cognitive impairment.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes. It uses advanced sequencing technology to identify genetic variations or mutations that may be associated with a particular disorder, such as Sneddon syndrome.

In the context of Sneddon syndrome, an NGS genetic test for the ADA2 gene would involve sequencing the entire gene to identify any variations or mutations that may be present. This can help confirm a diagnosis of Sneddon syndrome and provide important information for treatment and management of the condition.

It is important to note that genetic testing for Sneddon syndrome and other genetic disorders should be performed by a qualified healthcare professional or genetic counselor, who can interpret the results and provide appropriate guidance and support.