ATXN10 Gene Spinocerebellar Ataxia Type 10 Autosomal Dominant Genetic Test
Test Name: ATXN10 Gene Spinocerebellar Ataxia Type 10 Autosomal Dominant Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
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: Neurological Disorders
Doctor: Neurologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for ATXN10 Gene Spinocerebellar Ataxia Type 10, Autosomal Dominant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ATXN10 Gene Spinocerebellar Ataxia Type 10, Autosomal Dominant.
Test Details: The ATXN10 gene is associated with a genetic disorder called spinocerebellar ataxia type 10 (SCA10). This disorder is characterized by progressive degeneration of the cerebellum, which leads to problems with coordination and balance. An autosomal dominant NGS genetic test refers to a genetic test that uses next-generation sequencing (NGS) technology to analyze the ATXN10 gene for mutations or variations. Autosomal dominant means that only one copy of the mutated gene is needed to cause the disorder, and NGS allows for the simultaneous sequencing of multiple genes, making it a more efficient and comprehensive testing method. The purpose of the ATXN10 gene spinocerebellar ataxia type 10 autosomal dominant NGS genetic test is to identify mutations or variations in the ATXN10 gene that may be responsible for causing spinocerebellar ataxia type 10. This information can help with diagnosis, prognosis, and genetic counseling for individuals and families affected by this disorder.
| Test Name | ATXN10 Gene Spinocerebellar ataxia type 10 autosomal dominant 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 ATXN10 Gene Spinocerebellar ataxia type 10, autosomal dominant NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ATXN10 Gene Spinocerebellar ataxia type 10, autosomal dominant |
| Test Details | The ATXN10 gene is associated with a genetic disorder called spinocerebellar ataxia type 10 (SCA10). This disorder is characterized by progressive degeneration of the cerebellum, which leads to problems with coordination and balance. An autosomal dominant NGS genetic test refers to a genetic test that uses next-generation sequencing (NGS) technology to analyze the ATXN10 gene for mutations or variations. Autosomal dominant means that only one copy of the mutated gene is needed to cause the disorder, and NGS allows for the simultaneous sequencing of multiple genes, making it a more efficient and comprehensive testing method. The purpose of the ATXN10 gene spinocerebellar ataxia type 10 autosomal dominant NGS genetic test is to identify mutations or variations in the ATXN10 gene that may be responsible for causing spinocerebellar ataxia type 10. This information can help with diagnosis, prognosis, and genetic counseling for individuals and families affected by this disorder. |
