UQCRQ Gene Mitochondrial Complex III Deficiency Genetic Test
Welcome to DNA Labs UAE, where we offer the UQCRQ Gene Mitochondrial Complex III Deficiency Genetic Test. This test is designed to identify mutations or variations in the UQCRQ gene or other genes associated with mitochondrial complex III deficiency. Read on to learn more about the test details, cost, symptoms, diagnosis, and more.
Test Components
- UQCRQ Gene Mitochondrial Complex III Deficiency Genetic Test
Price
The cost of the test is 4400.0 AED.
Sample Condition
We accept blood samples, extracted DNA, or one drop of blood on an FTA card.
Report Delivery
Test results are typically delivered within 3 to 4 weeks.
Method
The test is performed using NGS (Next-Generation Sequencing) technology.
Test Type
The UQCRQ Gene Mitochondrial Complex III Deficiency Genetic Test is specifically designed for neurological disorders.
Doctor
The test is recommended by neurologists.
Test Department
The test is conducted by our Genetics department.
Pre Test Information
Prior to the test, it is important to provide the clinical history of the patient who is going for the UQCRQ Gene Mitochondrial Complex III Deficiency NGS Genetic DNA Test. A genetic counseling session will also be conducted to draw a pedigree chart of family members affected by this condition.
Test Details
The UQCRQ gene is responsible for encoding a protein called ubiquinol-cytochrome c reductase complex III subunit 9. This protein is a crucial component of the mitochondrial complex III, which is an enzyme complex involved in the electron transport chain and ATP generation. Mitochondrial complex III deficiency refers to a condition where there is a defect in the function of this enzyme complex. This deficiency can lead to various symptoms, including muscle weakness, exercise intolerance, lactic acidosis, and neurological abnormalities.
NGS genetic testing is a method used to analyze multiple genes simultaneously, providing a comprehensive assessment of genetic variations. In the context of mitochondrial complex III deficiency, NGS genetic testing can be used to identify specific mutations or variations in the UQCRQ gene or other genes associated with this condition. This can help in confirming a diagnosis, predicting disease progression, and guiding treatment decisions.
It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate counseling and guidance based on the test results.
| Test Name | UQCRQ Gene Mitochondrial complex III 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 UQCRQ Gene Mitochondrial complex III deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with UQCRQ Gene Mitochondrial complex III deficiency |
| Test Details |
The UQCRQ gene is a gene that encodes a protein called ubiquinol-cytochrome c reductase complex III subunit 9, which is a component of the mitochondrial complex III. Mitochondrial complex III is a crucial enzyme complex involved in the electron transport chain, responsible for generating energy in the form of ATP. Mitochondrial complex III deficiency refers to a condition where there is a defect in the function of this enzyme complex. This deficiency can lead to a range of symptoms and clinical manifestations, including muscle weakness, exercise intolerance, lactic acidosis, and various neurological abnormalities. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, providing a comprehensive assessment of genetic variations. In the context of mitochondrial complex III deficiency, NGS genetic testing can be used to identify specific mutations or variations in the UQCRQ gene or other genes associated with this condition. This can help in confirming a diagnosis, predicting disease progression, and guiding treatment decisions. It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate counseling and guidance based on the test results. |
