FASTKD2 Gene Mitochondrial Complex IV Deficiency Genetic Test sale cost 4400 AED
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FASTKD2 Gene Mitochondrial Complex IV Deficiency Genetic Test Cost

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

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The FASTKD2 Gene Mitochondrial Complex IV Deficiency Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the FASTKD2 gene. These mutations can lead to mitochondrial complex IV deficiency, a rare genetic condition that affects cellular energy production. Mitochondrial complex IV, also known as cytochrome c oxidase, is essential for the final step of the mitochondrial respiratory chain, which generates ATP, the primary energy currency of the cell. Deficiencies in this complex can result in a wide range of symptoms, including muscle weakness, heart problems, and neurological issues, depending on the severity and specific tissues affected.

The test involves analyzing the patient’s DNA to look for specific genetic changes in the FASTKD2 gene that are known to cause the deficiency. It is a crucial tool for clinicians in the diagnosis and management of patients suspected of having mitochondrial disorders, allowing for a targeted approach to treatment and genetic counseling for affected families.

The cost of the FASTKD2 Gene Mitochondrial Complex IV Deficiency Genetic Test at DNA Labs UAE is 4400 AED. Given the complexity of mitochondrial diseases and the specialized nature of this genetic test, it represents a valuable investment in accurately diagnosing and managing conditions related to mitochondrial dysfunction.

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FASTKD2 Gene Mitochondrial complex IV deficiency Genetic Test

Test Details

FASTKD2 gene is associated with mitochondrial complex IV deficiency, which is a genetic disorder that affects the function of mitochondria, specifically complex IV of the electron transport chain. This deficiency leads to impaired energy production and can cause various symptoms including muscle weakness, developmental delay, intellectual disability, and organ dysfunction. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genome. It allows for the simultaneous analysis of multiple genes, including FASTKD2, to identify any mutations or variants that may be present. This type of testing can help diagnose mitochondrial complex IV deficiency and provide valuable information for treatment and management of the condition.

Test Name

FASTKD2 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

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 FASTKD2 Gene Mitochondrial complex IV deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FASTKD2 Gene Mitochondrial complex IV deficiency.

Test Name FASTKD2 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 FASTKD2 Gene Mitochondrial complex IV deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FASTKD2 Gene Mitochondrial complex IV deficiency
Test Details

FASTKD2 gene is associated with mitochondrial complex IV deficiency, which is a genetic disorder that affects the function of mitochondria, specifically complex IV of the electron transport chain. This deficiency leads to impaired energy production and can cause various symptoms including muscle weakness, developmental delay, intellectual disability, and organ dysfunction.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genome. It allows for the simultaneous analysis of multiple genes, including FASTKD2, to identify any mutations or variants that may be present. This type of testing can help diagnose mitochondrial complex IV deficiency and provide valuable information for treatment and management of the condition.

SKU: TEST-1708 Category:

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