CTNNA2 Gene Neuronal Migration Disorder Genetic Test sale cost 4400 AED
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CTNNA2 Gene Neuronal Migration Disorder Genetic Test Cost

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

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The CTNNA2 gene is associated with critical functions in the nervous system, playing a vital role in the process of neuronal migration, a fundamental phase in brain development. Mutations in the CTNNA2 gene can lead to various neurological disorders, emphasizing the importance of genetic testing for early diagnosis and intervention.

The CTNNA2 Gene Neuronal Migration Disorder Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the CTNNA2 gene. This test is crucial for individuals who may have neurological conditions related to impaired neuronal migration, as it can provide definitive genetic evidence of such disorders. Early detection through this test can facilitate timely medical and therapeutic interventions, potentially improving patient outcomes.

The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the CTNNA2 gene. DNA Labs UAE, renowned for its commitment to precision and excellence in genetic diagnostics, ensures that this test is conducted under the highest standards of quality and reliability. By opting for this test, patients and their families can gain valuable insights into their genetic makeup, paving the way for personalized treatment strategies and better understanding of their conditions.

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CTNNA2 Gene Neuronal migration disorder 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 CTNNA2 Gene Neuronal migration disorder NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CTNNA2 Gene Neuronal migration disorder.

Test Details

The CTNNA2 gene is associated with a disorder known as neuronal migration disorder. Neuronal migration refers to the process by which nerve cells, or neurons, move from their place of origin to their final location in the brain during fetal development. Disruptions in this process can lead to various neurological disorders.

Next-generation sequencing (NGS) is a genetic testing method that allows for the rapid sequencing of large amounts of DNA. It can be used to identify mutations or variations in genes, including the CTNNA2 gene, that may be associated with neuronal migration disorders.

NGS genetic testing for CTNNA2 gene mutations can help in the diagnosis and management of individuals with neuronal migration disorders. It can also provide valuable information for genetic counseling and family planning.

It is important to note that genetic testing should be done under the guidance of a healthcare professional who specializes in genetics. They can help interpret the results and provide appropriate recommendations based on the individual’s specific situation.

Test Name CTNNA2 Gene Neuronal migration disorder 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 CTNNA2 Gene Neuronal migration disorder NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CTNNA2 Gene Neuronal migration disorder
Test Details

The CTNNA2 gene is associated with a disorder known as neuronal migration disorder. Neuronal migration refers to the process by which nerve cells, or neurons, move from their place of origin to their final location in the brain during fetal development. Disruptions in this process can lead to various neurological disorders.

Next-generation sequencing (NGS) is a genetic testing method that allows for the rapid sequencing of large amounts of DNA. It can be used to identify mutations or variations in genes, including the CTNNA2 gene, that may be associated with neuronal migration disorders.

NGS genetic testing for CTNNA2 gene mutations can help in the diagnosis and management of individuals with neuronal migration disorders. It can also provide valuable information for genetic counseling and family planning.

It is important to note that genetic testing should be done under the guidance of a healthcare professional who specializes in genetics. They can help interpret the results and provide appropriate recommendations based on the individual’s specific situation.

SKU: TEST-1850 Category:

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