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MT-ND3 Gene Leigh syndrome due to mitochondrial complex I deficiency Genetic Test

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

-21%

Leigh syndrome due to mitochondrial complex I deficiency is a severe neurological disorder that arises from genetic mutations affecting mitochondrial function, particularly the activity of complex I, a crucial enzyme in the mitochondrial respiratory chain. The MT-ND3 gene is one of the genes implicated in this condition. Mutations in the MT-ND3 gene can lead to impaired energy production in cells, resulting in the wide range of symptoms associated with Leigh syndrome, including developmental delay, muscle weakness, and breathing difficulties.

To diagnose this specific cause of Leigh syndrome, genetic testing is available at DNA Labs UAE. The test focuses on identifying mutations in the MT-ND3 gene that are known to contribute to mitochondrial complex I deficiency. This targeted genetic testing is crucial for confirming the diagnosis, understanding the disease’s progression, and guiding treatment decisions.

The cost of the MT-ND3 gene Leigh syndrome due to mitochondrial complex I deficiency genetic test at DNA Labs UAE is 4400 AED. This investment covers the analysis of the MT-ND3 gene to detect mutations associated with the condition. By choosing this test, patients and their families can gain valuable insights into the genetic underpinnings of the disease, enabling more personalized and effective management strategies.

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MT-ND3 Gene Leigh syndrome due to mitochondrial complex I deficiency Genetic Test

Components: MT-ND3 Gene Leigh syndrome due to 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-ND3 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-ND3 Gene Leigh syndrome due to mitochondrial complex I deficiency.

Test Details:

The MT-ND3 gene is one of the genes that make up the mitochondrial DNA (mtDNA) and is involved in the production of a subunit of the mitochondrial complex I enzyme. Leigh syndrome is a rare genetic disorder characterized by a progressive degeneration of the central nervous system, leading to developmental delay, muscle weakness, movement disorders, and respiratory problems. Mitochondrial complex I deficiency refers to a defect in the function of the mitochondrial complex I enzyme, which is responsible for the first step in the electron transport chain, a crucial process in cellular energy production. Mutations in the MT-ND3 gene can lead to a deficiency in complex I function, resulting in Leigh syndrome.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify genetic variations or mutations that may be associated with a particular disorder. In the context of Leigh syndrome due to mitochondrial complex I deficiency, NGS genetic testing can be used to analyze the MT-ND3 gene and other genes involved in mitochondrial function to identify any mutations or variations that may be causing the disease. By identifying the specific genetic mutations responsible for Leigh syndrome due to mitochondrial complex I deficiency, NGS genetic testing can help with accurate diagnosis, prognosis, and potential treatment options. It can also provide valuable information for genetic counseling and family planning.

Test Name MT-ND3 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-ND3 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-ND3 Gene Leigh syndrome due to mitochondrial complex I deficiency
Test Details

The MT-ND3 gene is one of the genes that make up the mitochondrial DNA (mtDNA) and is involved in the production of a subunit of the mitochondrial complex I enzyme. Leigh syndrome is a rare genetic disorder characterized by a progressive degeneration of the central nervous system, leading to developmental delay, muscle weakness, movement disorders, and respiratory problems.

Mitochondrial complex I deficiency refers to a defect in the function of the mitochondrial complex I enzyme, which is responsible for the first step in the electron transport chain, a crucial process in cellular energy production. Mutations in the MT-ND3 gene can lead to a deficiency in complex I function, resulting in Leigh syndrome.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify genetic variations or mutations that may be associated with a particular disorder. In the context of Leigh syndrome due to mitochondrial complex I deficiency, NGS genetic testing can be used to analyze the MT-ND3 gene and other genes involved in mitochondrial function to identify any mutations or variations that may be causing the disease.

By identifying the specific genetic mutations responsible for Leigh syndrome due to mitochondrial complex I deficiency, NGS genetic testing can help with accurate diagnosis, prognosis, and potential treatment options. It can also provide valuable information for genetic counseling and family planning.