Sale!

Leigh Syndrome and Mitochondrial Encephalopathy Gene Panel Test

Original price was: 9,600 د.إ.Current price is: 7,200 د.إ.

-25%

Leigh Syndrome, also known as Mitochondrial Encephalopathy, is a severe neurological disorder that typically arises in the first year of life. This condition is characterized by progressive loss of mental and movement abilities, which can lead to severe neurological and physical impairment. Leigh Syndrome is caused by genetic mutations affecting the mitochondria, the energy-producing structures within cells, leading to energy production failure and, subsequently, cell death, particularly in the brain, muscles, and heart.

To diagnose this complex condition, a Mitochondrial Encephalopathy Gene Panel Test is utilized. This comprehensive genetic test screens for mutations in multiple genes known to be associated with Leigh Syndrome and other mitochondrial disorders. By examining a broad panel of genes, this test provides a more accurate diagnosis, guiding treatment options and management strategies for affected individuals.

The test is available at DNA Labs UAE, a leading facility in genetic testing and diagnostics. The cost of the Mitochondrial Encephalopathy Gene Panel Test is 7200 AED. Conducting the test in a specialized and reputable laboratory like DNA Labs UAE ensures high accuracy and reliability of the results, which is crucial for the effective management of Leigh Syndrome and related mitochondrial disorders. This test is a critical step in the journey towards understanding and managing these complex conditions, offering hope for affected families through precise diagnosis and the potential for targeted therapies.

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
Guaranteed Safe Checkout

Leigh Syndrome and Mitochondrial Encephalopathy Gene Panel Test

Cost: AED 7200.0

Test Name: Leigh Syndrome and Mitochondrial Encephalopathy Gene Panel Test

Components: Sterile container/ Sterile Normal Saline Container/EDTA Vacutainer(3 ml)

Price: 7200.0 AED

Sample Condition: Amniotic fluid/ Chorionic villi/ Peripheral blood

Report Delivery: 4-6 weeks

Method: NGS

Test type: Genetics

Doctor: General Physician

Test Department:

Pre Test Information: Leigh Syndrome & Mitochondrial Encephalopathy Gene Panel can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Test Details

The Leigh Syndrome & Mitochondrial Encephalopathy Gene Panel is a genetic test that analyzes a group of genes associated with Leigh syndrome and mitochondrial encephalopathy. These are rare genetic disorders that affect the function of the mitochondria, which are responsible for producing energy in cells.

Leigh syndrome is a progressive neurological disorder that usually appears in infancy or early childhood. It can cause symptoms such as developmental delay, muscle weakness, seizures, and breathing difficulties. Mitochondrial encephalopathy is a broader term that encompasses a range of disorders that affect the brain and nervous system due to mitochondrial dysfunction.

The gene panel test analyzes a set of genes that have been associated with Leigh syndrome and mitochondrial encephalopathy, including MT-ATP6, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND6, MT-CO1, MT-CO2, MT-CO3, MT-CYB, NDUFA1, NDUFA2, NDUFA4, NDUFA5, NDUFA6, NDUFA8, NDUFA9, NDUFA10, NDUFB3, NDUFB4, NDUFB8, NDUFB9, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS6, NDUFS7, NDUFS8, SDHA, SDHB, SDHC, SDHD, SUCLG1, and SURF1.

By analyzing these genes, the test can identify mutations or variations that may be causing or contributing to Leigh syndrome or mitochondrial encephalopathy. This information can help with diagnosis, prognosis, and treatment planning for affected individuals and their families.

Test Name Leigh Syndrome and Mitochondrial Encephalopathy Gene Panel Test
Components Sterile container/ Sterile Normal Saline Container/EDTA Vacutainer(3 ml)
Price 7200.0 AED
Sample Condition Amniotic fluid\/ Chorionic villi\/ Peripheral blood
Report Delivery 4-6 weeks
Method NGS
Test type Genetics
Doctor General Physician
Test Department:
Pre Test Information Leigh Syndrome & Mitochondrial Encephalopathy Gene Panel can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

The Leigh Syndrome & Mitochondrial Encephalopathy Gene Panel is a genetic test that analyzes a group of genes associated with Leigh syndrome and mitochondrial encephalopathy. These are rare genetic disorders that affect the function of the mitochondria, which are responsible for producing energy in cells.

Leigh syndrome is a progressive neurological disorder that usually appears in infancy or early childhood. It can cause symptoms such as developmental delay, muscle weakness, seizures, and breathing difficulties. Mitochondrial encephalopathy is a broader term that encompasses a range of disorders that affect the brain and nervous system due to mitochondrial dysfunction.

The gene panel test analyzes a set of genes that have been associated with Leigh syndrome and mitochondrial encephalopathy, including MT-ATP6, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND6, MT-CO1, MT-CO2, MT-CO3, MT-CYB, NDUFA1, NDUFA2, NDUFA4, NDUFA5, NDUFA6, NDUFA8, NDUFA9, NDUFA10, NDUFB3, NDUFB4, NDUFB8, NDUFB9, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS6, NDUFS7, NDUFS8, SDHA, SDHB, SDHC, SDHD, SUCLG1, and SURF1.

By analyzing these genes, the test can identify mutations or variations that may be causing or contributing to Leigh syndrome or mitochondrial encephalopathy. This information can help with diagnosis, prognosis, and treatment planning for affected individuals and their families.