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MT-CO3 Gene Mitochondrial Complex IV Deficiency Genetic Test Cost

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

-21%

The “MT-CO3 Gene Mitochondrial Complex IV Deficiency Genetic Test” is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the MT-CO3 gene. This gene plays a critical role in the functioning of Complex IV, also known as cytochrome c oxidase, which is essential for the mitochondrial respiratory chain’s energy production. Mutations in the MT-CO3 gene can lead to mitochondrial complex IV deficiency, a condition that affects multiple body systems and can result in a wide range of symptoms, including muscle weakness, heart problems, and neurological issues.

This genetic test is crucial for individuals who present symptoms suggestive of mitochondrial disorders or have a family history of such conditions. Early detection through this test can aid in the diagnosis, management, and treatment planning for affected individuals. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for mutations in the MT-CO3 gene.

The cost of the MT-CO3 Gene Mitochondrial Complex IV Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the specialized nature of the test and the sophisticated technology and expertise required to accurately identify mutations in the MT-CO3 gene. Patients considering this test should consult with their healthcare provider to understand its benefits and implications fully.

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MT-CO3 Gene Mitochondrial complex IV deficiency 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 MT-CO3 Gene Mitochondrial complex IV deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-CO3 Gene Mitochondrial complex IV deficiency.

Test Details

MT-CO3 gene is one of the genes that encode for a subunit of the mitochondrial complex IV, also known as cytochrome c oxidase. Mitochondrial complex IV is an enzyme complex involved in the electron transport chain, which is essential for cellular respiration and energy production.

Mitochondrial complex IV deficiency refers to a condition where there is a dysfunction or deficiency in the activity of this enzyme complex. This deficiency can be caused by mutations in various genes, including the MT-CO3 gene.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the context of mitochondrial complex IV deficiency, NGS genetic testing can be used to identify mutations or variations in the MT-CO3 gene or other genes associated with this condition.

NGS genetic testing can provide valuable information about the genetic basis of mitochondrial complex IV deficiency, helping to diagnose the condition and guide treatment decisions. It can also be used for carrier testing, prenatal testing, or genetic counseling for individuals and families at risk of having or transmitting this genetic disorder.

Test Name MT-CO3 Gene Mitochondrial complex IV deficiency 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 MT-CO3 Gene Mitochondrial complex IV deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-CO3 Gene Mitochondrial complex IV deficiency
Test Details

MT-CO3 gene is one of the genes that encode for a subunit of the mitochondrial complex IV, also known as cytochrome c oxidase. Mitochondrial complex IV is an enzyme complex involved in the electron transport chain, which is essential for cellular respiration and energy production.

Mitochondrial complex IV deficiency refers to a condition where there is a dysfunction or deficiency in the activity of this enzyme complex. This deficiency can be caused by mutations in various genes, including the MT-CO3 gene.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the context of mitochondrial complex IV deficiency, NGS genetic testing can be used to identify mutations or variations in the MT-CO3 gene or other genes associated with this condition.

NGS genetic testing can provide valuable information about the genetic basis of mitochondrial complex IV deficiency, helping to diagnose the condition and guide treatment decisions. It can also be used for carrier testing, prenatal testing, or genetic counseling for individuals and families at risk of having or transmitting this genetic disorder.