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COX20 Gene Ataxia and Muscle Hypotonia Genetic Test

Name: COX20 Gene Ataxia and Muscle Hypotonia Genetic Test
SKU: TEST-1070
Price: 4400 AED
Availability: InStock

4,400 د.إ

-21%

The “COX20 Gene Ataxia and Muscle Hypotonia Genetic Test” is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the COX20 gene, which are associated with certain neurodegenerative disorders. Ataxia, characterized by a lack of muscle control during voluntary movements, and muscle hypotonia, a condition marked by reduced muscle tone, can both result from anomalies in the COX20 gene. This gene plays a crucial role in the proper functioning of the mitochondria, the powerhouse of the cell, and its mutations can lead to a variety of mitochondrial disorders.

The test, priced at 4400 AED, involves collecting a DNA sample from the patient, typically through a blood draw or a cheek swab. The genetic material is then analyzed using advanced sequencing technologies to identify any mutations in the COX20 gene. Results from this test can provide crucial information for the diagnosis, management, and treatment planning for individuals exhibiting symptoms of ataxia and muscle hypotonia, potentially guiding families towards appropriate genetic counseling and support services. DNA Labs UAE ensures confidentiality and accuracy in the testing process, offering a comprehensive approach to understanding genetic contributions to these complex conditions.

Description

COX20 Gene Ataxia and Muscle Hypotonia Genetic Test

Test Name: COX20 Gene Ataxia and Muscle Hypotonia 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 COX20 Gene Ataxia and Muscle Hypotonia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with COX20 Gene Ataxia and Muscle Hypotonia.

Test Details:

The COX20 gene is responsible for encoding a protein that is essential for the proper function of the mitochondria, which are the energy-producing structures within cells. Mutations in the COX20 gene can lead to a variety of mitochondrial disorders, including ataxia and muscle hypotonia.

NGS (next-generation sequencing) genetic testing is a type of genetic testing that uses advanced technology to analyze multiple genes simultaneously. This type of testing can be useful in identifying the specific genetic mutation responsible for a particular disorder, including those associated with the COX20 gene.

If a person is suspected to have a mitochondrial disorder, including ataxia and muscle hypotonia, their healthcare provider may recommend NGS genetic testing to identify any mutations in the COX20 gene or other genes related to mitochondrial function. This information can help with diagnosis and treatment planning.

Test Name	COX20 Gene Ataxia and muscle hypotonia 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 COX20 Gene Ataxia and muscle hypotonia NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with COX20 Gene Ataxia and muscle hypotonia
Test Details	The COX20 gene is responsible for encoding a protein that is essential for the proper function of the mitochondria, which are the energy-producing structures within cells. Mutations in the COX20 gene can lead to a variety of mitochondrial disorders, including ataxia and muscle hypotonia. NGS (next-generation sequencing) genetic testing is a type of genetic testing that uses advanced technology to analyze multiple genes simultaneously. This type of testing can be useful in identifying the specific genetic mutation responsible for a particular disorder, including those associated with the COX20 gene. If a person is suspected to have a mitochondrial disorder, including ataxia and muscle hypotonia, their healthcare provider may recommend NGS genetic testing to identify any mutations in the COX20 gene or other genes related to mitochondrial function. This information can help with diagnosis and treatment planning.