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MT-ND6 Gene Leigh syndrome due to 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 Leigh Syndrome due to Mitochondrial Complex I Deficiency Genetic Test” is a specialized diagnostic assessment offered by DNA Labs UAE. Priced at 4400 AED, this test is designed to identify mutations in the MT-ND6 gene, which are associated with Leigh syndrome stemming from mitochondrial complex I deficiency. Leigh syndrome is a severe neurological disorder that typically emerges in infancy or early childhood, characterized by progressive loss of mental and movement abilities. Mitochondrial complex I deficiency is one of the most common biochemical causes of this condition. The test involves analyzing the patient’s DNA to detect any genetic anomalies in the MT-ND6 gene, aiding in the accurate diagnosis of Leigh syndrome. This information is crucial for understanding the disease’s progression, potential treatment options, and genetic counseling for affected families. DNA Labs UAE provides this service with a focus on accuracy, confidentiality, and support for patients and their families navigating the complexities of genetic disorders.

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MT-ND6 Gene Leigh Syndrome due to Mitochondrial Complex I Deficiency Genetic Test

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 MT-ND6 Gene Leigh syndrome due to 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 Leigh syndrome due to mitochondrial complex I deficiency.

Test Details

The MT-ND6 gene is a gene that encodes for a subunit of mitochondrial complex I, which is involved in the production of energy within cells. Leigh syndrome is a rare genetic disorder characterized by progressive neurological deterioration, typically appearing in infancy or early childhood. Mitochondrial complex I deficiency refers to a dysfunction or impairment of the mitochondrial complex I enzyme, which is responsible for the first step in the electron transport chain. This deficiency can lead to a decreased production of energy in cells, particularly in tissues with high energy demands such as the brain and muscles.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous sequencing of multiple genes or even the entire genome. It is a powerful tool for identifying genetic mutations or variations that may be responsible for certain diseases or conditions. In the context of Leigh syndrome due to mitochondrial complex I deficiency, an NGS genetic test would involve sequencing the MT-ND6 gene, as well as other relevant genes involved in mitochondrial function or energy production.

The aim of this test would be to identify any mutations or variations in these genes that may be contributing to the development of Leigh syndrome in an individual. By identifying the specific genetic cause of Leigh syndrome in an individual, NGS genetic testing can help with diagnosis, provide valuable information for prognosis and management, and potentially inform reproductive decisions for affected individuals and their families.

Test Name MT-ND6 Gene Leigh syndrome due to 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 Leigh syndrome due to 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 Leigh syndrome due to mitochondrial complex I deficiency
Test Details

The MT-ND6 gene is a gene that encodes for a subunit of mitochondrial complex I, which is involved in the production of energy within cells. Leigh syndrome is a rare genetic disorder characterized by progressive neurological deterioration, typically appearing in infancy or early childhood.

Mitochondrial complex I deficiency refers to a dysfunction or impairment of the mitochondrial complex I enzyme, which is responsible for the first step in the electron transport chain. This deficiency can lead to a decreased production of energy in cells, particularly in tissues with high energy demands such as the brain and muscles.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous sequencing of multiple genes or even the entire genome. It is a powerful tool for identifying genetic mutations or variations that may be responsible for certain diseases or conditions.

In the context of Leigh syndrome due to mitochondrial complex I deficiency, an NGS genetic test would involve sequencing the MT-ND6 gene, as well as other relevant genes involved in mitochondrial function or energy production. The aim of this test would be to identify any mutations or variations in these genes that may be contributing to the development of Leigh syndrome in an individual.

By identifying the specific genetic cause of Leigh syndrome in an individual, NGS genetic testing can help with diagnosis, provide valuable information for prognosis and management, and potentially inform reproductive decisions for affected individuals and their families.

SKU: TEST-1498