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ATXN10 Gene Spinocerebellar Ataxia Type 10 Autosomal Dominant Genetic Test Cost

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

-21%

The ATXN10 gene is associated with Spinocerebellar Ataxia Type 10 (SCA10), a disorder characterized by progressive coordination problems due to the degeneration of the cerebellum in the brain. This condition is inherited in an autosomal dominant pattern, meaning a single copy of the altered gene in each cell is sufficient to cause the disorder. The ATXN10 gene test is a crucial diagnostic tool for identifying mutations within the ATXN10 gene, helping in the diagnosis of SCA10. This genetic test is available at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the ATXN10 gene test at DNA Labs UAE is 4400 AED. This test can provide individuals and families with essential information regarding the genetic basis of Spinocerebellar Ataxia Type 10, facilitating informed decisions about management and care for affected individuals.

Description

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.