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MT-ATP6 Gene Mitochondrial Complex V ATP Synthase Deficiency Genetic Test

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

-21%

The “MT-ATP6 Gene Mitochondrial Complex V ATP Synthase Deficiency Genetic Test” is a specialized diagnostic examination offered by DNA Labs UAE, designed to detect mutations in the MT-ATP6 gene. This gene plays a critical role in the normal functioning of mitochondrial complex V, also known as ATP synthase. ATP synthase is essential for ATP production, the main energy currency in cells. Mutations in the MT-ATP6 gene can lead to mitochondrial disorders, which are complex and can affect multiple systems in the body, often with severe outcomes.

This test is particularly important for individuals showing symptoms suggestive of mitochondrial diseases or for those with a family history of such conditions. Early and accurate diagnosis through this genetic test can aid in the management of the disease, allowing for tailored treatments and interventions to improve quality of life.

The test is conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services. The cost of the test is 4400 AED, which reflects the sophisticated nature of the analysis and the invaluable insights it provides into the patient’s genetic health, particularly concerning mitochondrial function.

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MT-ATP6 Gene Mitochondrial complex V ATP synthase deficiency Genetic Test

Test Name: MT-ATP6 Gene Mitochondrial complex V ATP synthase 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-ATP6 Gene Mitochondrial complex V (ATP synthase) deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-ATP6 Gene Mitochondrial complex V (ATP synthase) deficiency.

Test Details

MT-ATP6 gene mitochondrial complex V (ATP synthase) deficiency is a genetic disorder that affects the function of the ATP synthase enzyme, which is involved in the production of ATP (adenosine triphosphate) in the mitochondria. This deficiency can lead to a variety of symptoms, including muscle weakness, exercise intolerance, developmental delays, and neurological problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of MT-ATP6 gene mitochondrial complex V deficiency, NGS genetic testing can be used to identify mutations or variations in the MT-ATP6 gene that may be responsible for the disorder.

NGS genetic testing involves the extraction of DNA from a patient’s sample (usually blood or saliva), followed by the sequencing of the MT-ATP6 gene using advanced sequencing platforms. The resulting sequence data is then compared to a reference sequence to identify any genetic variations or mutations that may be present.

This type of genetic testing can provide valuable information for diagnosis, prognosis, and treatment decisions for individuals suspected of having MT-ATP6 gene mitochondrial complex V deficiency. It can also help identify carriers of the disorder and provide information for family planning purposes.

It’s important to note that NGS genetic testing may not be available in all healthcare settings and may require specialized laboratories or genetic testing centers. Additionally, the interpretation of the test results should be done by a qualified healthcare professional or genetic counselor who can provide appropriate counseling and guidance based on the specific genetic findings.

Test Name MT-ATP6 Gene Mitochondrial complex V ATP synthase 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-ATP6 Gene Mitochondrial complex V (ATP synthase) deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-ATP6 Gene Mitochondrial complex V (ATP synthase) deficiency
Test Details

MT-ATP6 gene mitochondrial complex V (ATP synthase) deficiency is a genetic disorder that affects the function of the ATP synthase enzyme, which is involved in the production of ATP (adenosine triphosphate) in the mitochondria. This deficiency can lead to a variety of symptoms, including muscle weakness, exercise intolerance, developmental delays, and neurological problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of MT-ATP6 gene mitochondrial complex V deficiency, NGS genetic testing can be used to identify mutations or variations in the MT-ATP6 gene that may be responsible for the disorder.

NGS genetic testing involves the extraction of DNA from a patient’s sample (usually blood or saliva), followed by the sequencing of the MT-ATP6 gene using advanced sequencing platforms. The resulting sequence data is then compared to a reference sequence to identify any genetic variations or mutations that may be present.

This type of genetic testing can provide valuable information for diagnosis, prognosis, and treatment decisions for individuals suspected of having MT-ATP6 gene mitochondrial complex V deficiency. It can also help identify carriers of the disorder and provide information for family planning purposes.

It’s important to note that NGS genetic testing may not be available in all healthcare settings and may require specialized laboratories or genetic testing centers. Additionally, the interpretation of the test results should be done by a qualified healthcare professional or genetic counselor who can provide appropriate counseling and guidance based on the specific genetic findings.

SKU: TEST-1711 Category:

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