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SYNE1 Gene Spinocerebellar Ataxia Type 8 Autosomal Recessive Genetic Test Cost

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

-21%

The SYNE1 gene is associated with a condition known as Spinocerebellar Ataxia Type 8 (SCA8), which is a genetic disorder characterized by progressive problems with movement. This condition primarily affects the cerebellum, the part of the brain that controls coordination and balance. Symptoms of SCA8 may include uncoordinated movements, trouble walking, and issues with speech. It is an autosomal recessive disorder, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected by the condition.

To diagnose this condition, a specific genetic test is available at DNA Labs UAE, which focuses on identifying mutations in the SYNE1 gene that are responsible for SCA8. The test is crucial for confirming the diagnosis, understanding the risk of passing the condition to the next generation, and guiding management and treatment decisions. The cost of the SYNE1 gene Spinocerebellar Ataxia Type 8 Autosomal Recessive Genetic Test at DNA Labs UAE is 4400 AED. This test is a valuable resource for individuals with a family history of SCA8 or those exhibiting symptoms of the disorder, providing them with critical information about their genetic health.

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SYNE1 Gene Spinocerebellar Ataxia Type 8 Autosomal Recessive Genetic Test

Are you concerned about Spinocerebellar Ataxia Type 8 (SCA8)? DNA Labs UAE offers a comprehensive genetic test to identify mutations or variations in the SYNE1 gene that may be associated with the development of SCA8. Our advanced Next-generation sequencing (NGS) technology allows us to analyze multiple genes simultaneously, providing accurate and reliable results.

Test Details

The SYNE1 gene is associated with Spinocerebellar Ataxia Type 8 (SCA8), an autosomal dominant neurodegenerative disorder that affects the cerebellum and spinal cord. Although SCA8 is typically inherited in an autosomal dominant manner, our genetic test can help identify potential mutations or variations in the SYNE1 gene.

Test Name: SYNE1 Gene Spinocerebellar Ataxia Type 8 Autosomal Recessive Genetic Test

  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the SYNE1 Gene Spinocerebellar Ataxia Type 8 Autosomal Recessive 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 SCA8. This will help us understand the inheritance pattern and provide accurate results.

Consult a Healthcare Professional

It is crucial to consult with a healthcare professional or a genetic counselor for accurate and comprehensive information about genetic testing for SCA8. They can provide detailed insights into the testing process, its limitations, and the implications of the test results. Our team of experienced neurologists and geneticists is here to support you throughout the testing process and provide the necessary guidance.

Don’t let uncertainties about SCA8 weigh you down. Contact DNA Labs UAE today to schedule your SYNE1 Gene Spinocerebellar Ataxia Type 8 Autosomal Recessive Genetic Test and take control of your health.

Test Name SYNE1 Gene Spinocerebellar ataxia type 8 autosomal recessive Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SYNE1 Gene Spinocerebellar ataxia type 8, autosomal recessive NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SYNE1 Gene Spinocerebellar ataxia type 8, autosomal recessive
Test Details

The SYNE1 gene is associated with Spinocerebellar Ataxia Type 8 (SCA8), an autosomal dominant neurodegenerative disorder that affects the cerebellum and spinal cord. However, it is important to note that SCA8 is typically inherited in an autosomal dominant manner, not autosomal recessive.

Next-generation sequencing (NGS) genetic tests are a type of genetic test that can analyze multiple genes simultaneously. In the context of SCA8, an NGS genetic test can be used to identify mutations or variations in the SYNE1 gene that may be associated with the development of SCA8.

However, it is crucial to consult with a healthcare professional or a genetic counselor for accurate and comprehensive information about genetic testing for SCA8. They can provide detailed insights into the testing process, its limitations, and the implications of the test results.

SKU: TEST-2082 Category:

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