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CP Gene Cerebellar Ataxia Genetic Test

4,400 د.إ

-21%

The CP Gene Cerebellar Ataxia Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the CP gene that are associated with the development of cerebellar ataxia. Cerebellar ataxia is a neurological disorder characterized by a lack of muscle coordination, which can affect speech, eye movements, the ability to swallow, walking, and other voluntary movements. This condition is often inherited and can be caused by mutations in various genes, including the CP gene.

The test is conducted through a comprehensive analysis of the patient’s DNA, extracted from a blood sample, to detect specific genetic alterations in the CP gene that are known to contribute to the condition. The results from this test can provide crucial information for the diagnosis, management, and understanding of the individual’s condition. It can also offer insights into the risk of passing the condition on to future generations, aiding in family planning decisions.

Priced at 4400 AED, the CP Gene Cerebellar Ataxia Genetic Test at DNA Labs UAE represents a significant investment in personal health and genetic understanding. It is a valuable resource for individuals showing symptoms of cerebellar ataxia or those with a family history of the disorder, offering them a clearer picture of their genetic health and enabling them to take informed steps towards managing their condition.

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  • This test is not intended for medical diagnosis or treatment
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CP Gene Cerebellar Ataxia Genetic Test

Test Components: CP Gene Cerebellar Ataxia Genetic Test

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 CP Gene Cerebellar ataxia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CP Gene Cerebellar ataxia.

Test Details:

The CP Gene Cerebellar Ataxia NGS Genetic Test is a genetic test that analyzes the CP gene for mutations that can cause cerebellar ataxia. Cerebellar ataxia is a neurological disorder that affects coordination and balance, and can be caused by a variety of genetic mutations. The CP gene provides instructions for making a protein called ceruloplasmin, which helps to regulate the levels of copper in the body. Mutations in the CP gene can lead to a buildup of copper in the brain, which can cause damage to the cerebellum and result in cerebellar ataxia. The NGS (Next-Generation Sequencing) technology used in this test allows for the rapid and accurate analysis of multiple genes simultaneously, making it a powerful tool for diagnosing genetic disorders like cerebellar ataxia.

Test Name CP Gene Cerebellar ataxia 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 CP Gene Cerebellar ataxia NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CP Gene Cerebellar ataxia
Test Details

The CP Gene Cerebellar Ataxia NGS Genetic Test is a genetic test that analyzes the CP gene for mutations that can cause cerebellar ataxia. Cerebellar ataxia is a neurological disorder that affects coordination and balance, and can be caused by a variety of genetic mutations. The CP gene provides instructions for making a protein called ceruloplasmin, which helps to regulate the levels of copper in the body. Mutations in the CP gene can lead to a buildup of copper in the brain, which can cause damage to the cerebellum and result in cerebellar ataxia. The NGS (Next-Generation Sequencing) technology used in this test allows for the rapid and accurate analysis of multiple genes simultaneously, making it a powerful tool for diagnosing genetic disorders like cerebellar ataxia.