ANO10 Gene Spinocerebellar Ataxia Type 10 Autosomal Recessive Genetic Test
Welcome to DNA Labs UAE, your trusted genetic lab for all your testing needs. Today, we would like to discuss the ANO10 Gene Spinocerebellar Ataxia Type 10 Autosomal Recessive Genetic Test.
Test Details
The ANO10 gene is associated with a type of spinocerebellar ataxia called spinocerebellar ataxia type 10 (SCA10). This genetic disorder is characterized by progressive problems with coordination and balance, resulting in unsteady movements and difficulties with walking.
The ANO10 gene is inherited in an autosomal recessive manner, which means that an individual must inherit two copies of the mutated gene (one from each parent) in order to develop the disorder. If an individual inherits only one mutated copy of the ANO10 gene, they are considered a carrier and typically do not show symptoms of the disorder.
NGS (Next-Generation Sequencing) genetic testing can be used to analyze an individual’s DNA and identify any mutations or variations in the ANO10 gene. This type of testing can help confirm a diagnosis of SCA10 and provide information about the genetic basis of the disorder.
It is important to note that genetic testing for SCA10 is typically performed in individuals who show symptoms of the disorder or have a family history of SCA10. The test results can help with making a diagnosis, providing information about disease progression and prognosis, and assisting with family planning decisions. Genetic counseling is often recommended before and after genetic testing to discuss the implications of the results.
Test Name: ANO10 Gene Spinocerebellar Ataxia Type 10 Autosomal Recessive 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
Neurological Disorders
Doctor
Neurologist
Test Department
Genetics
Pre Test Information
Clinical History of Patient who is going for ANO10 Gene Spinocerebellar Ataxia Type 10, autosomal recessive NGS Genetic DNA Test
A Genetic Counselling session to draw a pedigree chart of family members affected with ANO10 Gene Spinocerebellar Ataxia Type 10, autosomal recessive
Thank you for considering DNA Labs UAE for your genetic testing needs. If you have any further questions or would like to schedule an appointment, please don’t hesitate to contact us.
| Test Name | ANO10 Gene Spinocerebellar ataxia type 10 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 ANO10 Gene Spinocerebellar ataxia type 10, autosomal recessive NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ANO10 Gene Spinocerebellar ataxia type 10, autosomal recessive |
| Test Details |
The ANO10 gene is associated with a type of spinocerebellar ataxia called spinocerebellar ataxia type 10 (SCA10). This genetic disorder is characterized by progressive problems with coordination and balance, resulting in unsteady movements and difficulties with walking. The ANO10 gene is inherited in an autosomal recessive manner, which means that an individual must inherit two copies of the mutated gene (one from each parent) in order to develop the disorder. If an individual inherits only one mutated copy of the ANO10 gene, they are considered a carrier and typically do not show symptoms of the disorder. NGS (Next-Generation Sequencing) genetic testing can be used to analyze an individual’s DNA and identify any mutations or variations in the ANO10 gene. This type of testing can help confirm a diagnosis of SCA10 and provide information about the genetic basis of the disorder. It is important to note that genetic testing for SCA10 is typically performed in individuals who show symptoms of the disorder or have a family history of SCA10. The test results can help with making a diagnosis, providing information about disease progression and prognosis, and assisting with family planning decisions. Genetic counseling is often recommended before and after genetic testing to discuss the implications of the results. |
