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PLEKHG4 Gene Spinocerebellar Ataxia Type 4 Autosomal Dominant Genetic Test Cost

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

-21%

The PLEKHG4 gene is associated with Spinocerebellar Ataxia Type 4 (SCA4), a rare genetic disorder characterized by progressive problems with movement. This condition is part of a group of genetic disorders known as spinocerebellar ataxias, which are caused by degeneration of the cerebellum and spinal cord, leading to coordination and balance difficulties. SCA4 specifically is inherited in an autosomal dominant manner, meaning only one copy of the altered gene in each cell is sufficient to cause the disorder.

To diagnose SCA4, genetic testing is crucial. DNA Labs UAE offers a specific genetic test that identifies mutations in the PLEKHG4 gene, which can confirm a diagnosis of Spinocerebellar Ataxia Type 4. This test is particularly important for individuals with a family history of the condition or those exhibiting symptoms related to coordination and balance.

The cost of the PLEKHG4 Gene Spinocerebellar Ataxia Type 4 Autosomal Dominant Genetic Test at DNA Labs UAE is 4400 AED. This test is a significant step towards a definitive diagnosis, enabling affected individuals and their families to understand their condition better and manage it more effectively through appropriate therapeutic interventions and genetic counseling.

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PLEKHG4 Gene Spinocerebellar ataxia type 4 autosomal dominant Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab offering the PLEKHG4 Gene Spinocerebellar ataxia type 4 autosomal dominant Genetic Test.

Test Components

  • Price: 4400.0 AED

Sample Condition

We accept blood samples, extracted DNA, or one drop of blood on FTA Card.

Report Delivery

Your test results will be delivered within 3 to 4 weeks.

Method

We utilize NGS (Next-Generation Sequencing) technology for this genetic test.

Test Type

This test is specifically designed for Neurological Disorders.

Doctor

Your test will be conducted by a qualified Neurologist.

Test Department

This test is conducted in our Genetics department.

Pre Test Information

Before the test, we require the clinical history of the patient who is going for the PLEKHG4 Gene Spinocerebellar ataxia type 4 autosomal dominant Genetic Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with this genetic disorder.

Test Details

Spinocerebellar ataxia type 4 (SCA4) is an autosomal dominant genetic disorder that affects the cerebellum and spinal cord. It is caused by mutations in the PLEKHG4 gene. NGS genetic testing is a method used to analyze multiple genes simultaneously. In the case of SCA4, NGS can be used to identify mutations or variations in the PLEKHG4 gene that may be responsible for the development of the disorder.

The NGS genetic test for SCA4 involves obtaining a DNA sample, usually through a blood sample or cheek swab, from the individual being tested. The DNA is then sequenced using NGS technology to identify any mutations or variations in the PLEKHG4 gene. The results of the test can help confirm a diagnosis of SCA4 and provide information about the specific mutation present in the gene.

It is important to note that genetic testing for SCA4 should be conducted by a qualified healthcare professional or genetic counselor who can provide appropriate counseling and support. They can help interpret the results and discuss the implications of the test for the individual and their family members.

Test Name PLEKHG4 Gene Spinocerebellar ataxia type 4 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 PLEKHG4 Gene Spinocerebellar ataxia type 4, autosomal dominant NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PLEKHG4 Gene Spinocerebellar ataxia type 4, autosomal dominant
Test Details

Spinocerebellar ataxia type 4 (SCA4) is an autosomal dominant genetic disorder that affects the cerebellum and spinal cord. It is caused by mutations in the PLEKHG4 gene.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the case of SCA4, NGS can be used to identify mutations or variations in the PLEKHG4 gene that may be responsible for the development of the disorder.

The NGS genetic test for SCA4 involves obtaining a DNA sample, usually through a blood sample or cheek swab, from the individual being tested. The DNA is then sequenced using NGS technology to identify any mutations or variations in the PLEKHG4 gene. The results of the test can help confirm a diagnosis of SCA4 and provide information about the specific mutation present in the gene.

It is important to note that genetic testing for SCA4 should be conducted by a qualified healthcare professional or genetic counselor who can provide appropriate counseling and support. They can help interpret the results and discuss the implications of the test for the individual and their family members.

SKU: TEST-2076 Category:

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