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MT-ND6 Gene Mitochondrial Complex I Deficiency Genetic Test Cost

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

-21%

The MT-ND6 gene plays a crucial role in the mitochondrial complex I, which is essential for the mitochondrial respiratory chain. This chain is responsible for producing energy in cells. Mutations in the MT-ND6 gene can lead to mitochondrial complex I deficiency, a condition that affects various body systems, particularly the nervous system and muscles. Symptoms can range from muscle weakness and exercise intolerance to more severe neurodegenerative disorders.

To diagnose this condition, a genetic test targeting the MT-ND6 gene can be performed. This test looks for mutations in the MT-ND6 gene that are known to cause mitochondrial complex I deficiency. It is a critical step for confirming the diagnosis, understanding the disease’s progression, and managing it effectively.

In the UAE, DNA Labs UAE offers this specific genetic test. The cost of the test is 4400 AED. Conducting the test at DNA Labs UAE ensures that patients receive accurate and reliable results, thanks to their state-of-the-art facilities and experienced genetic professionals. This test is crucial for patients suspected of having mitochondrial complex I deficiency, as it can guide treatment options and help in the management of symptoms.

Description

MT-ND6 Gene Mitochondrial complex I deficiency Genetic Test

Components: MT-ND6 Gene Mitochondrial complex I 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-ND6 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-ND6 Gene Mitochondrial complex I deficiency.

Test Details:

MT-ND6 gene mitochondrial complex I deficiency is a condition characterized by a mutation in the MT-ND6 gene, which is part of the mitochondrial DNA. This gene provides instructions for producing a protein that is essential for the function of complex I in the mitochondria, which is involved in energy production.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of MT-ND6 gene mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations or variants in the MT-ND6 gene and other genes involved in complex I function.

NGS genetic testing can provide valuable information about the specific genetic cause of mitochondrial complex I deficiency, which can help in making an accurate diagnosis and determining appropriate treatment options. It can also be used for carrier testing and prenatal testing in families with a known mutation in the MT-ND6 gene.

Overall, NGS genetic testing for MT-ND6 gene mitochondrial complex I deficiency can help in understanding the underlying genetic basis of the condition and guide personalized management and treatment strategies.

Test Name	MT-ND6 Gene Mitochondrial complex I 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-ND6 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-ND6 Gene Mitochondrial complex I deficiency
Test Details	MT-ND6 gene mitochondrial complex I deficiency is a condition characterized by a mutation in the MT-ND6 gene, which is part of the mitochondrial DNA. This gene provides instructions for producing a protein that is essential for the function of complex I in the mitochondria, which is involved in energy production. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of MT-ND6 gene mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations or variants in the MT-ND6 gene and other genes involved in complex I function. NGS genetic testing can provide valuable information about the specific genetic cause of mitochondrial complex I deficiency, which can help in making an accurate diagnosis and determining appropriate treatment options. It can also be used for carrier testing and prenatal testing in families with a known mutation in the MT-ND6 gene. Overall, NGS genetic testing for MT-ND6 gene mitochondrial complex I deficiency can help in understanding the underlying genetic basis of the condition and guide personalized management and treatment strategies.