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ANO10 Gene Spinocerebellar Ataxia Type 10 Autosomal Recessive Genetic Test Cost

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

-21%

The ANO10 gene is associated with a rare form of Spinocerebellar Ataxia, specifically Type 10 (SCA10), which is an autosomal recessive genetic disorder. This condition is characterized by progressive degeneration of the cerebellum, leading to coordination and balance difficulties, among other symptoms. Given the hereditary nature of SCA10, genetic testing is a crucial tool for diagnosis, family planning, and understanding the risk of transmission to offspring.

DNA Labs UAE offers a comprehensive genetic test targeting the ANO10 gene to identify mutations that cause Spinocerebellar Ataxia Type 10. This test is particularly important for individuals with a family history of SCA10 or those exhibiting symptoms suggestive of the condition. The genetic test is priced at 4400 AED and involves analyzing DNA samples to detect the presence of specific mutations in the ANO10 gene that are known to cause the disorder. By confirming a diagnosis through genetic testing, affected individuals can receive appropriate counseling, consider their options for management and treatment, and make informed decisions about family planning.

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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.

SKU: TEST-2052 Category:

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