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ATP2B3 Gene Spinocerebellar Ataxia Type 1 X-Linked Genetic Test Cost

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

-21%

The ATP2B3 Gene Spinocerebellar Ataxia Type 1 X-Linked Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the ATP2B3 gene, which are linked to the development of Spinocerebellar Ataxia Type 1 (SCA1), a condition affecting the cerebellum and leading to progressive coordination problems. This particular form of ataxia is inherited in an X-linked pattern, meaning the gene responsible for the condition is located on the X chromosome.

SCA1 is characterized by a range of symptoms, including difficulty with coordination and balance, speech impairments, and eye movement abnormalities. Early detection through genetic testing can be crucial for managing the condition, allowing for personalized treatment plans and genetic counseling for affected families.

The test is conducted at DNA Labs UAE, a leading facility in genetic diagnostics and research. The cost for the ATP2B3 Gene Spinocerebellar Ataxia Type 1 X-Linked Genetic Test is 4400 AED. The process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the lab for the presence of mutations in the ATP2B3 gene. Results from this test can provide invaluable information for affected individuals and their families regarding the management of the condition and the risk of transmission to future generations.

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ATP2B3 Gene Spinocerebellar Ataxia Type 1 X-linked Genetic Test

Are you concerned about Spinocerebellar Ataxia Type 1? DNA Labs UAE offers the ATP2B3 Gene Spinocerebellar Ataxia Type 1 X-linked Genetic Test to provide you with valuable insights into this genetic disorder.

Test Components and Price

Test Name: ATP2B3 Gene Spinocerebellar Ataxia Type 1 X-linked 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

Clinical History of Patient who is going for ATP2B3 Gene Spinocerebellar Ataxia Type 1, X-linked NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with ATP2B3 Gene Spinocerebellar Ataxia Type 1, X-linked

Test Details

The ATP2B3 gene is associated with Spinocerebellar Ataxia Type 1, which is a genetic disorder characterized by progressive degeneration of the cerebellum and other parts of the nervous system. This condition is inherited in an X-linked manner, meaning it primarily affects males.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of Spinocerebellar Ataxia Type 1, an NGS genetic test would involve sequencing the ATP2B3 gene to identify any mutations or variants that may be causing or contributing to the disease.

By analyzing the ATP2B3 gene, NGS genetic testing can help diagnose Spinocerebellar Ataxia Type 1 and provide valuable information for genetic counseling and management of the condition. It can also be used to identify carriers of the gene mutation, which can be important for family planning and reproductive decisions.

It is important to consult with a healthcare professional or a genetic counselor to discuss the appropriateness and availability of NGS genetic testing for Spinocerebellar Ataxia Type 1, as well as the potential implications and limitations of the test results.

Test Name ATP2B3 Gene Spinocerebellar ataxia type 1 X-linked 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 ATP2B3 Gene Spinocerebellar ataxia type 1, X-linked NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ATP2B3 Gene Spinocerebellar ataxia type 1, X-linked
Test Details

The ATP2B3 gene is associated with Spinocerebellar ataxia type 1, which is a genetic disorder characterized by progressive degeneration of the cerebellum and other parts of the nervous system. This condition is inherited in an X-linked manner, meaning it primarily affects males.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of Spinocerebellar ataxia type 1, an NGS genetic test would involve sequencing the ATP2B3 gene to identify any mutations or variants that may be causing or contributing to the disease.

By analyzing the ATP2B3 gene, NGS genetic testing can help diagnose Spinocerebellar ataxia type 1 and provide valuable information for genetic counseling and management of the condition. It can also be used to identify carriers of the gene mutation, which can be important for family planning and reproductive decisions.

It is important to consult with a healthcare professional or a genetic counselor to discuss the appropriateness and availability of NGS genetic testing for Spinocerebellar ataxia type 1, as well as the potential implications and limitations of the test results.

SKU: TEST-2050

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