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NDUFAF5 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 NDUFAF5 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 in cells. Mutations in the NDUFAF5 gene can lead to mitochondrial complex I deficiency, a genetic disorder that affects various body systems, particularly the nervous system and muscles, leading to a wide range of health issues.

To diagnose this condition, a genetic test specifically targeting the NDUFAF5 gene can be conducted. This test is crucial for identifying mutations in the gene, confirming a diagnosis, and guiding treatment and management decisions. It involves collecting a DNA sample, typically through a blood draw, which is then analyzed in a laboratory for any genetic abnormalities associated with mitochondrial complex I deficiency.

In the UAE, DNA Labs UAE offers this specialized genetic test. The cost of the NDUFAF5 Gene Mitochondrial Complex I Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This state-of-the-art facility ensures accurate and reliable testing, employing the latest in genetic testing technology and methodologies. The test not only aids in the diagnosis but also plays a role in family planning and understanding the risk of recurrence in future pregnancies.

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  • This test is not intended for medical diagnosis or treatment
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NDUFAF5 Gene Mitochondrial Complex I Deficiency Genetic Test

At DNA Labs UAE, we offer the NDUFAF5 Gene Mitochondrial Complex I Deficiency Genetic Test to diagnose and manage mitochondrial complex I deficiency, a genetic disorder characterized by dysfunction in the mitochondrial respiratory chain complex I.

Test Details

The NDUFAF5 gene is associated with mitochondrial complex I deficiency, which is responsible for the first step in the electron transport chain, generating energy for the cell. Our Next-Generation Sequencing (NGS) technology allows for a comprehensive analysis of the NDUFAF5 gene to identify any mutations or variations that may be present.

NGS genetic tests are highly accurate and can analyze multiple genes simultaneously, providing a comprehensive assessment of genetic variations. This helps in the diagnosis and management of mitochondrial complex I deficiency, as well as providing information about the inheritance pattern and the risk of passing the condition on to future generations.

Components and Price

  • Test Name: NDUFAF5 Gene Mitochondrial Complex I Deficiency Genetic Test
  • Price: 4400.0 AED

Sample Condition and Report Delivery

We accept blood or extracted DNA samples for this test. Alternatively, one drop of blood can be collected on an FTA card. The report will be delivered within 3 to 4 weeks.

Test Type and Doctor

This test falls under the category of Neurological Disorders and is recommended by Neurologists. Our dedicated test department for Genetics ensures accurate and reliable results.

Pre Test Information

Before undergoing the NDUFAF5 Gene Mitochondrial Complex I Deficiency Genetic Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by NDUFAF5 Gene Mitochondrial Complex I Deficiency.

Consultation and Management

It is crucial to consult with a healthcare professional or genetic counselor to understand the implications of NDUFAF5 gene mutations and the results of an NGS genetic test. They can provide guidance on interpreting the test results and assist in developing an appropriate management plan.

Test Name NDUFAF5 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 NDUFAF5 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFAF5 Gene Mitochondrial complex I deficiency
Test Details

NDUFAF5 gene is associated with mitochondrial complex I deficiency, which is a genetic disorder characterized by a dysfunction in the mitochondrial respiratory chain complex I. This complex is responsible for the first step in the electron transport chain, which generates energy for the cell.

A Next-Generation Sequencing (NGS) genetic test can be performed to analyze the NDUFAF5 gene and identify any mutations or variations that may be present. This test involves sequencing the DNA of an individual to identify any changes in the NDUFAF5 gene that may be contributing to mitochondrial complex I deficiency.

NGS genetic tests are highly accurate and can analyze multiple genes simultaneously, allowing for a comprehensive assessment of genetic variations. This can help in the diagnosis and management of mitochondrial complex I deficiency, as well as provide information about the inheritance pattern and risk of passing the condition on to future generations.

It is important to consult with a healthcare professional or genetic counselor to understand the implications of NDUFAF5 gene mutations and the results of an NGS genetic test. They can provide guidance on the interpretation of the test results and help develop an appropriate management plan.

SKU: TEST-1689 Category:

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