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NDUFV1 Gene Mitochondrial Complex I Deficiency Genetic Test Cost

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

-21%

The NDUFV1 gene plays a crucial role in the mitochondrial complex I, a key enzyme complex necessary for the mitochondrial respiratory chain’s proper function, which is vital for cellular energy production. Mutations in the NDUFV1 gene can lead to mitochondrial complex I deficiency, a condition that can cause a wide range of clinical manifestations, including neurological disorders, muscle weakness, and metabolic problems. Given the complexity and variability of symptoms, accurate diagnosis is essential for appropriate management and treatment of the condition.

The NDUFV1 Gene Mitochondrial Complex I Deficiency Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to detect mutations in the NDUFV1 gene that could lead to mitochondrial complex I deficiency. This genetic testing is crucial for individuals exhibiting symptoms suggestive of mitochondrial disorders or those with a family history of such conditions, as it can provide definitive diagnosis, guide treatment options, and help in understanding the risk of passing the condition to offspring.

The test is conducted using a sample of the patient’s blood or other tissues, where DNA is extracted and analyzed for specific mutations in the NDUFV1 gene. The process is meticulous, ensuring high accuracy and reliability of the results.

The cost of the NDUFV1 Gene Mitochondrial Complex I Deficiency Genetic Test at DNA Labs UAE is 4400 AED. While the cost may seem significant, the value of obtaining a precise diagnosis cannot be overstated, as it opens the door to targeted treatments and interventions, potentially improving the quality of life for those affected by mitochondrial complex I deficiency.

Description

NDUFV1 Gene Mitochondrial complex I deficiency Genetic Test

Components: NDUFV1 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 NDUFV1 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFV1 Gene Mitochondrial complex I deficiency.

Test Details:

The NDUFV1 gene is responsible for providing instructions to build a protein called NADH dehydrogenase (ubiquinone) flavoprotein 1, which is a subunit of the mitochondrial complex I enzyme. Mitochondrial complex I is involved in the process of oxidative phosphorylation, which generates energy in the form of ATP.

Mitochondrial complex I deficiency refers to a condition where there is a malfunction or reduced activity of the mitochondrial complex I enzyme. This deficiency can lead to a wide range of symptoms and can affect various organs and systems in the body.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. It allows for the detection of genetic variations, such as mutations or deletions, in the NDUFV1 gene. This type of testing can help diagnose mitochondrial complex I deficiency caused by NDUFV1 gene mutations.

By identifying specific genetic variations in the NDUFV1 gene, NGS genetic testing can provide important information about the underlying cause of mitochondrial complex I deficiency. This can help guide treatment options and management strategies for affected individuals.

Test Name	NDUFV1 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 NDUFV1 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFV1 Gene Mitochondrial complex I deficiency
Test Details	The NDUFV1 gene is responsible for providing instructions to build a protein called NADH dehydrogenase (ubiquinone) flavoprotein 1, which is a subunit of the mitochondrial complex I enzyme. Mitochondrial complex I is involved in the process of oxidative phosphorylation, which generates energy in the form of ATP. Mitochondrial complex I deficiency refers to a condition where there is a malfunction or reduced activity of the mitochondrial complex I enzyme. This deficiency can lead to a wide range of symptoms and can affect various organs and systems in the body. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. It allows for the detection of genetic variations, such as mutations or deletions, in the NDUFV1 gene. This type of testing can help diagnose mitochondrial complex I deficiency caused by NDUFV1 gene mutations. By identifying specific genetic variations in the NDUFV1 gene, NGS genetic testing can provide important information about the underlying cause of mitochondrial complex I deficiency. This can help guide treatment options and management strategies for affected individuals.