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MT-CO3 Gene Cytochrome C Oxidase 3 Deficiency Genetic Test

4,400 د.إ

-21%

The MT-CO3 gene is responsible for encoding a crucial subunit of cytochrome c oxidase, which is part of the mitochondrial respiratory chain complex IV. This enzyme complex plays a vital role in the process of oxidative phosphorylation, where cells produce ATP, the primary energy currency of the cell. Mutations or deficiencies in the MT-CO3 gene can disrupt this process, leading to a variety of mitochondrial disorders that can affect multiple systems in the body, particularly those with high energy demands such as the nervous system and muscles.

The Cytochrome C Oxidase 3 Deficiency Genetic Test is a specialized diagnostic tool designed to identify mutations in the MT-CO3 gene. This test is crucial for individuals who exhibit symptoms suggestive of mitochondrial disorders, including muscle weakness, neurological deficits, and heart problems, among others. Early and accurate diagnosis through this genetic testing can aid in the management of the condition, allowing for targeted treatments and interventions that can improve quality of life and outcomes for affected individuals.

The test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. DNA Labs UAE employs state-of-the-art technology and expertise to deliver accurate and reliable genetic testing results. The cost of the Cytochrome C Oxidase 3 Deficiency Genetic Test is 4400 AED, reflecting the comprehensive analysis and the specialized nature of the test. This investment can be invaluable for families seeking answers to complex health issues related to mitochondrial dysfunction and offers a pathway towards personalized medical care based on genetic insights.

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MT-CO3 Gene Cytochrome c oxidase 3 deficiency Genetic Test

Components: MT-CO3 Gene Cytochrome c oxidase 3 deficiency 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 MT-CO3 Gene Cytochrome c oxidase 3 deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-CO3 Gene Cytochrome c oxidase 3 deficiency.

Test Details

The MT-CO3 gene codes for the cytochrome c oxidase subunit III, which is a key component of the mitochondrial respiratory chain. Mutations in this gene can lead to cytochrome c oxidase 3 deficiency, which is a rare genetic disorder that affects the function of the mitochondrial respiratory chain. This can cause a range of symptoms, including muscle weakness, exercise intolerance, developmental delay, and neurological problems.

NGS genetic testing can be used to identify mutations in the MT-CO3 gene and diagnose cytochrome c oxidase 3 deficiency. This involves sequencing the entire gene to identify any variations or mutations that may be causing the disorder. NGS testing is a highly accurate and efficient method of genetic testing that can provide a definitive diagnosis for patients with suspected genetic disorders. It can also be used for carrier testing and prenatal testing in families with a history of cytochrome c oxidase 3 deficiency.

Test Name MT-CO3 Gene Cytochrome c oxidase 3 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 Cytochrome c oxidase 3 deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-CO3 Gene Cytochrome c oxidase 3 deficiency
Test Details

The MT-CO3 gene codes for the cytochrome c oxidase subunit III, which is a key component of the mitochondrial respiratory chain. Mutations in this gene can lead to cytochrome c oxidase 3 deficiency, which is a rare genetic disorder that affects the function of the mitochondrial respiratory chain. This can cause a range of symptoms, including muscle weakness, exercise intolerance, developmental delay, and neurological problems.

NGS genetic testing can be used to identify mutations in the MT-CO3 gene and diagnose cytochrome c oxidase 3 deficiency. This involves sequencing the entire gene to identify any variations or mutations that may be causing the disorder. NGS testing is a highly accurate and efficient method of genetic testing that can provide a definitive diagnosis for patients with suspected genetic disorders. It can also be used for carrier testing and prenatal testing in families with a history of cytochrome c oxidase 3 deficiency.