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Mitochondrial Mutation Detection Comprehensive Panel Test

5,620 د.إ

-10%

The Mitochondrial Mutation Detection Comprehensive Panel Test, offered by DNA Labs UAE, is a sophisticated diagnostic tool designed to identify mutations within the mitochondrial DNA (mtDNA). This test is particularly significant for individuals experiencing symptoms or with a family history of mitochondrial disorders, as it helps in the accurate diagnosis of such conditions. Mitochondrial diseases can manifest in various forms and affect multiple systems of the body, making early and precise detection crucial for effective management and treatment.

Priced at 5620 AED, the test employs advanced genetic sequencing technologies to examine the entire mitochondrial genome. This thorough analysis enables the identification of both common and rare mutations that could lead to mitochondrial dysfunction. By pinpointing the specific genetic alterations responsible for a patient’s condition, healthcare providers can tailor treatment strategies more effectively, offer prognostic insights, and advise on the risk of passing the condition to future generations.

Conducted at DNA Labs UAE, a facility known for its cutting-edge genetic testing services, the Mitochondrial Mutation Detection Comprehensive Panel Test is a testament to the lab’s commitment to providing high-quality, accurate diagnostic solutions. Patients opting for this test can expect professional service, confidentiality, and comprehensive support throughout the testing process.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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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.

SKU: TEST-827 Category:

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