NDUFS4 Gene Mitochondrial Complex I Deficiency Genetic Test sale cost 4400 AED
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NDUFS4 Gene Mitochondrial Complex I Deficiency Genetic Test Cost

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

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The NDUFS4 gene plays a crucial role in the proper functioning of mitochondrial complex I, a vital component of the mitochondrial respiratory chain responsible for energy production within cells. Mutations in the NDUFS4 gene can lead to mitochondrial complex I deficiency, a severe genetic disorder that affects multiple systems in the body, including the nervous system and muscles, leading to a range of health issues such as muscle weakness, neurological deficits, and in severe cases, early childhood mortality.

The NDUFS4 Gene Mitochondrial Complex I Deficiency Genetic Test is a specialized diagnostic tool designed to detect mutations in the NDUFS4 gene. This test is critical for the accurate diagnosis of mitochondrial complex I deficiency, enabling healthcare providers to tailor treatment and management strategies to the specific needs of affected individuals. Early diagnosis through genetic testing can significantly improve the quality of life for patients and their families by allowing for timely interventions and support.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test offers a comprehensive analysis of the NDUFS4 gene. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experts in the field of genetic testing, ensuring high-quality and reliable results.

The cost of the NDUFS4 Gene Mitochondrial Complex I Deficiency Genetic Test is 4400 AED. While the price may seem high, the test provides invaluable information for the management of mitochondrial complex I deficiency, making it a worthwhile investment in the health and well-being of affected individuals.

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NDUFS4 Gene Mitochondrial Complex I Deficiency Genetic Test

Components:

  • Test Name: NDUFS4 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 NDUFS4 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFS4 Gene Mitochondrial Complex I Deficiency.

Test Details:

NDUFS4 gene mitochondrial complex I deficiency is a rare genetic disorder that affects the function of mitochondria, the energy-producing structures within cells. This condition is caused by mutations in the NDUFS4 gene, which provides instructions for making a protein that is a subunit of complex I, an essential component of the mitochondrial electron transport chain.

A next-generation sequencing (NGS) genetic test can be used to identify mutations in the NDUFS4 gene. NGS is a high-throughput sequencing technology that allows for the rapid and simultaneous sequencing of multiple genes or even the entire genome. It can detect various types of genetic variations, including small point mutations, insertions, deletions, and duplications.

The NGS genetic test for NDUFS4 gene mitochondrial complex I deficiency involves collecting a sample of DNA, usually through a blood or saliva sample. The DNA is then sequenced using NGS technology, and the resulting data is analyzed to identify any mutations or variations in the NDUFS4 gene.

The test results can help confirm a diagnosis of NDUFS4 gene mitochondrial complex I deficiency and provide information about the specific genetic mutation causing the condition. This information can be valuable for understanding the underlying cause of the disorder, predicting disease progression, and informing potential treatment options.

It is important to note that genetic testing should be done in consultation with a healthcare professional or genetic counselor who can provide guidance on the implications of the test results and help interpret them in the context of an individual’s specific situation.

Test Name NDUFS4 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 NDUFS4 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFS4 Gene Mitochondrial complex I deficiency
Test Details

NDUFS4 gene mitochondrial complex I deficiency is a rare genetic disorder that affects the function of mitochondria, the energy-producing structures within cells. This condition is caused by mutations in the NDUFS4 gene, which provides instructions for making a protein that is a subunit of complex I, an essential component of the mitochondrial electron transport chain.

A next-generation sequencing (NGS) genetic test can be used to identify mutations in the NDUFS4 gene. NGS is a high-throughput sequencing technology that allows for the rapid and simultaneous sequencing of multiple genes or even the entire genome. It can detect various types of genetic variations, including small point mutations, insertions, deletions, and duplications.

The NGS genetic test for NDUFS4 gene mitochondrial complex I deficiency involves collecting a sample of DNA, usually through a blood or saliva sample. The DNA is then sequenced using NGS technology, and the resulting data is analyzed to identify any mutations or variations in the NDUFS4 gene.

The test results can help confirm a diagnosis of NDUFS4 gene mitochondrial complex I deficiency and provide information about the specific genetic mutation causing the condition. This information can be valuable for understanding the underlying cause of the disorder, predicting disease progression, and informing potential treatment options.

It is important to note that genetic testing should be done in consultation with a healthcare professional or genetic counselor who can provide guidance on the implications of the test results and help interpret them in the context of an individual’s specific situation.

SKU: TEST-1693