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NDUFV2 Gene Mitochondrial Complex I Deficiency Genetic Test Cost

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

-21%

The NDUFV2 gene plays a crucial role in the mitochondrial complex I, which is a key enzyme complex in the mitochondrial electron transport chain responsible for energy production. Mutations in the NDUFV2 gene can lead to mitochondrial complex I deficiency, a condition that affects mitochondrial function and can result in a wide range of clinical symptoms, including neurodegenerative disorders, muscle weakness, and metabolic problems.

To diagnose this genetic condition, DNA Labs UAE offers a specialized genetic test targeting the NDUFV2 gene. This test is designed to identify mutations in the NDUFV2 gene that may lead to mitochondrial complex I deficiency. It involves collecting a DNA sample, usually through a blood draw or a cheek swab, and analyzing the genetic material for specific mutations associated with the condition.

The cost of the NDUFV2 gene mitochondrial complex I deficiency genetic test at DNA Labs UAE is 4400 AED. This price includes the cost of the sample collection, genetic analysis, and a comprehensive report that provides detailed insights into the patient’s genetic makeup with respect to the NDUFV2 gene. The test is conducted in a state-of-the-art laboratory by experienced geneticists and clinicians who specialize in mitochondrial diseases and genetics.

This genetic test is an important tool for diagnosing mitochondrial complex I deficiency, enabling healthcare providers to tailor treatment and management strategies to the specific needs of the patient. It can also provide valuable information for family planning and the assessment of risk in family members.

Description

NDUFV2 Gene Mitochondrial complex I deficiency Genetic Test

Components: NDUFV2 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 NDUFV2 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFV2 Gene Mitochondrial complex I deficiency.

Test Details: The NDUFV2 gene is responsible for providing instructions to make a protein that is a subunit of the mitochondrial complex I enzyme. Mitochondrial complex I is involved in the process of oxidative phosphorylation, which is essential for the production of energy in cells. A deficiency in mitochondrial complex I can lead to a variety of symptoms and health issues, including neurological problems, muscle weakness, developmental delays, and metabolic abnormalities.

Genetic testing using Next-Generation Sequencing (NGS) technology can be used to identify mutations or variations in the NDUFV2 gene that may be causing mitochondrial complex I deficiency. NGS genetic testing involves sequencing the DNA of an individual to identify any changes or variations in specific genes or regions of the genome. This technology allows for the simultaneous analysis of multiple genes, providing a comprehensive view of an individual’s genetic makeup.

By identifying mutations or variations in the NDUFV2 gene through NGS genetic testing, healthcare professionals can diagnose mitochondrial complex I deficiency and provide appropriate treatment and management strategies. This information can also be helpful for genetic counseling and family planning purposes.

Test Name	NDUFV2 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 NDUFV2 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFV2 Gene Mitochondrial complex I deficiency
Test Details	The NDUFV2 gene is responsible for providing instructions to make a protein that is a subunit of the mitochondrial complex I enzyme. Mitochondrial complex I is involved in the process of oxidative phosphorylation, which is essential for the production of energy in cells. A deficiency in mitochondrial complex I can lead to a variety of symptoms and health issues, including neurological problems, muscle weakness, developmental delays, and metabolic abnormalities. Genetic testing using Next-Generation Sequencing (NGS) technology can be used to identify mutations or variations in the NDUFV2 gene that may be causing mitochondrial complex I deficiency. NGS genetic testing involves sequencing the DNA of an individual to identify any changes or variations in specific genes or regions of the genome. This technology allows for the simultaneous analysis of multiple genes, providing a comprehensive view of an individual’s genetic makeup. By identifying mutations or variations in the NDUFV2 gene through NGS genetic testing, healthcare professionals can diagnose mitochondrial complex I deficiency and provide appropriate treatment and management strategies. This information can also be helpful for genetic counseling and family planning purposes.