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MT-CO1 Gene Cytochrome C Oxidase 1 Deficiency Genetic Test

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

-21%

The MT-CO1 gene, encoding for Cytochrome C Oxidase 1, plays a critical role in the mitochondrial respiratory chain, which is essential for energy production in cells. Deficiencies in this gene can lead to a range of mitochondrial disorders, characterized by symptoms such as muscle weakness, heart problems, and neurological issues. Early diagnosis through genetic testing is crucial for managing these conditions.

The MT-CO1 Gene Cytochrome C Oxidase 1 Deficiency Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the MT-CO1 gene. This test is pivotal for individuals exhibiting symptoms of mitochondrial disorders or those with a family history of such conditions, as it can provide definitive diagnosis and guide treatment options.

The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for any genetic abnormalities in the MT-CO1 gene. The process is highly accurate and provides vital information for the management of the associated conditions.

The cost of the MT-CO1 Gene Cytochrome C Oxidase 1 Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This investment can be crucial for individuals seeking insights into their genetic health, potentially leading to early intervention and better management of mitochondrial disorders.

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MT-CO1 Gene Cytochrome c oxidase 1 deficiency Genetic Test

Test Name: MT-CO1 Gene Cytochrome c oxidase 1 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-CO1 Gene Cytochrome c oxidase 1 deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-CO1 Gene Cytochrome c oxidase 1 deficiency

Test Details

The MT-CO1 gene encodes for the cytochrome c oxidase subunit 1, which is an essential component of the mitochondrial respiratory chain. Cytochrome c oxidase 1 deficiency is a rare genetic disorder that affects the function of this enzyme, leading to impaired energy production and mitochondrial dysfunction.

NGS (Next-Generation Sequencing) genetic testing is a powerful tool that can be used to identify mutations in the MT-CO1 gene that cause cytochrome c oxidase 1 deficiency. This test involves sequencing the entire coding region of the MT-CO1 gene and analyzing the data for genetic variations that may be associated with the disorder.

NGS genetic testing for cytochrome c oxidase 1 deficiency can help to confirm a diagnosis, provide information about the severity of the condition, and guide treatment decisions. It may also be used to identify carriers of the genetic mutation, which can be useful for family planning purposes.

Overall, NGS genetic testing for MT-CO1 gene mutations is an important tool for the diagnosis and management of cytochrome c oxidase 1 deficiency, a rare genetic disorder that can have significant impacts on affected individuals and their families.

Test Name MT-CO1 Gene Cytochrome c oxidase 1 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-CO1 Gene Cytochrome c oxidase 1 deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-CO1 Gene Cytochrome c oxidase 1 deficiency
Test Details

MT-CO1 gene encodes for the cytochrome c oxidase subunit 1, which is an essential component of the mitochondrial respiratory chain. Cytochrome c oxidase 1 deficiency is a rare genetic disorder that affects the function of this enzyme, leading to impaired energy production and mitochondrial dysfunction.

NGS (Next-Generation Sequencing) genetic testing is a powerful tool that can be used to identify mutations in the MT-CO1 gene that cause cytochrome c oxidase 1 deficiency. This test involves sequencing the entire coding region of the MT-CO1 gene and analyzing the data for genetic variations that may be associated with the disorder.

NGS genetic testing for cytochrome c oxidase 1 deficiency can help to confirm a diagnosis, provide information about the severity of the condition, and guide treatment decisions. It may also be used to identify carriers of the genetic mutation, which can be useful for family planning purposes.

Overall, NGS genetic testing for MT-CO1 gene mutations is an important tool for the diagnosis and management of cytochrome c oxidase 1 deficiency, a rare genetic disorder that can have significant impacts on affected individuals and their families.