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MT-ND2 Gene Mitochondrial Complex I Deficiency Genetic Test

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

-21%

The “MT-ND2 Gene Mitochondrial Complex I Deficiency Genetic Test” is a specialized diagnostic procedure designed to identify mutations in the MT-ND2 gene, which is known to be associated with mitochondrial complex I deficiency. This condition is a type of mitochondrial disorder that affects the mitochondrial complex I – the first enzyme complex in the mitochondrial respiratory chain. Mutations in the MT-ND2 gene can lead to a variety of clinical manifestations, including neurodegenerative diseases, muscle weakness, and metabolic syndromes, making early and accurate diagnosis crucial for management and treatment.

Performed at DNA Labs UAE, a leading facility in genetic testing, this test offers a comprehensive analysis of the MT-ND2 gene to detect any genetic alterations that may contribute to mitochondrial complex I deficiency. With a cost of 4400 AED, the test is conducted using advanced molecular techniques to ensure high sensitivity and specificity, providing essential information for patients and healthcare providers to make informed decisions regarding the condition’s management. The result from this test can also help in understanding the genetic basis of the disorder, guiding treatment options, and offering genetic counseling for affected families.

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MT-ND2 Gene Mitochondrial Complex I Deficiency Genetic Test

Components: MT-ND2 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-ND2 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-ND2 Gene Mitochondrial Complex I Deficiency.

Test Details:

The MT-ND2 gene is one of the genes found in the mitochondrial DNA. Mitochondrial Complex I Deficiency is a genetic disorder that affects the function of complex I, which is responsible for the first step in the electron transport chain in mitochondria.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of MT-ND2 gene mitochondrial Complex I Deficiency, NGS genetic testing would involve sequencing the MT-ND2 gene to identify any mutations or variations that may be causing the deficiency.

This type of genetic testing can help diagnose mitochondrial Complex I Deficiency and identify specific mutations or variations in the MT-ND2 gene that may be contributing to the condition. It can also provide information about the inheritance pattern of the disorder, which can be helpful for family planning and genetic counseling.

Test Name MT-ND2 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-ND2 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-ND2 Gene Mitochondrial complex I deficiency
Test Details

The MT-ND2 gene is one of the genes found in the mitochondrial DNA. Mitochondrial complex I deficiency is a genetic disorder that affects the function of complex I, which is responsible for the first step in the electron transport chain in mitochondria.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of MT-ND2 gene mitochondrial complex I deficiency, NGS genetic testing would involve sequencing the MT-ND2 gene to identify any mutations or variations that may be causing the deficiency.

This type of genetic testing can help diagnose mitochondrial complex I deficiency and identify specific mutations or variations in the MT-ND2 gene that may be contributing to the condition. It can also provide information about the inheritance pattern of the disorder, which can be helpful for family planning and genetic counseling.