MITOCHONDRIAL MUTATION DETECTION COMPREHENSIVE PANEL Test
Are you experiencing symptoms of mitochondrial diseases? DNA Labs UAE offers the MITOCHONDRIAL MUTATION DETECTION COMPREHENSIVE PANEL Test to help diagnose and detect mutations that can cause these rare genetic disorders.
Test Details
The MITOCHONDRIAL MUTATION DETECTION COMPREHENSIVE PANEL Test is a genetic test that analyzes a person’s mitochondrial DNA (mtDNA) for mutations that can cause mitochondrial diseases. Mitochondrial diseases are a group of rare genetic disorders that affect the energy production of cells in the body.
The test uses next-generation sequencing technology to analyze the entire mtDNA genome for mutations. This comprehensive panel includes the following test components: ND1, ND4, ND5, ND6, TL1, MCTYB1, ATP6, and ATP8.
Symptoms and Diagnosis
If you are experiencing symptoms such as neurological disorders or genetic diseases, this test can help provide a diagnosis. Common mitochondrial diseases that can be detected through this test include Leigh syndrome, MELAS syndrome, and Kearns-Sayre syndrome.
It is important to consult with a neurologist or pediatrician if you suspect a mitochondrial disorder. They can refer you for the MITOCHONDRIAL MUTATION DETECTION COMPREHENSIVE PANEL Test to help determine the cause of your symptoms.
Test Cost and Sample Condition
The cost of the MITOCHONDRIAL MUTATION DETECTION COMPREHENSIVE PANEL Test is 5620.0 AED. To perform the test, a sample of 4 mL (2 mL minimum) of whole blood is required. The sample should be collected in a Lavender top (EDTA) tube and shipped refrigerated. It is important not to freeze the sample.
Please note that a duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory for this test.
Report Delivery and Method
The sample should be submitted by Monday at 9 am, and the report will be delivered on Friday. The MITOCHONDRIAL MUTATION DETECTION COMPREHENSIVE PANEL Test is performed using PCR and sequencing methods in the MOLECULAR DIAGNOSTICS department.
Pre Test Information
Prior to undergoing the MITOCHONDRIAL MUTATION DETECTION COMPREHENSIVE PANEL Test, it is important to complete the Genomics Clinical Information Requisition Form (Form 20). This form is mandatory for the test.
Don’t wait any longer to get answers about your symptoms. Contact DNA Labs UAE and inquire about the MITOCHONDRIAL MUTATION DETECTION COMPREHENSIVE PANEL Test today!
Test Name | MITOCHONDRIAL MUTATION DETECTION COMPREHENSIVE PANEL Test |
---|---|
Components | *ND1*ND4*ND5*ND6*TL1*MCTYB1 *ATP6*ATP8 |
Price | 5620.0 AED |
Sample Condition | 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory. |
Report Delivery | Sample Mon by 9 am; Report Fri |
Method | PCR, Sequencing |
Test type | Neurological disorders, Genetic diseases |
Doctor | Neurologist, Pediatrician |
Test Department: | MOLECULAR DIAGNOSTICS |
Pre Test Information | Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory. |
Test Details | The Mitochondrial Mutation Detection Comprehensive Panel Test is a genetic test that analyzes a person’s mitochondrial DNA (mtDNA) for mutations that can cause mitochondrial diseases. Mitochondrial diseases are a group of rare genetic disorders that affect the energy production of cells in the body. The test uses next-generation sequencing technology to analyze the entire mtDNA genome for mutations. The test can detect mutations that are associated with a wide range of mitochondrial diseases, including Leigh syndrome, MELAS syndrome, and Kearns-Sayre syndrome. The test can be used to diagnose mitochondrial diseases in patients with suspected mitochondrial disorders, and can also be used to identify carriers of mitochondrial mutations in families with a history of mitochondrial disease. |