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NUBPL Gene Leigh syndrome Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The NUBPL Gene Leigh Syndrome Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the NUBPL gene, which are associated with Leigh syndrome. Leigh syndrome is a severe neurological disorder that typically arises in the first year of life, characterized by progressive loss of mental and movement abilities. The condition can lead to serious health complications, including respiratory failure and lactic acidosis, making early and accurate diagnosis crucial for managing symptoms and improving quality of life.

The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed to identify any genetic abnormalities in the NUBPL gene. This gene plays a critical role in the mitochondrial respiratory chain, which is essential for energy production in cells. Mutations in this gene can disrupt normal cellular function and lead to the symptoms observed in Leigh syndrome.

Priced at 4400 AED, the NUBPL Gene Leigh Syndrome Genetic Test is an important resource for families with a history of the disorder or for individuals presenting symptoms suggestive of Leigh syndrome. By confirming a diagnosis, the test can guide healthcare providers in developing a tailored management plan that may include nutritional support, respiratory care, and other interventions aimed at improving patient outcomes. DNA Labs UAE ensures a reliable and accurate testing process, providing crucial information for affected individuals and their families.

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NUBPL Gene Leigh Syndrome Genetic Test

Components: NUBPL Gene Leigh syndrome Genetic Test

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

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 NUBPL Gene Leigh syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NUBPL Gene Leigh syndrome.

Test Details

The NUBPL gene is associated with Leigh syndrome, a rare genetic disorder that affects the central nervous system. Leigh syndrome is characterized by progressive neurological deterioration, muscle weakness, movement disorders, and respiratory problems.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes, including the NUBPL gene. NGS can identify specific mutations or variations in the NUBPL gene that may be responsible for Leigh syndrome. This testing method provides a comprehensive analysis of the entire gene, increasing the chances of identifying potential disease-causing variants.

The NGS genetic test for the NUBPL gene can be used to confirm a diagnosis of Leigh syndrome, particularly in cases where the clinical presentation is consistent with the disorder. It can also be used for carrier testing, prenatal testing, or to assess the risk of passing the disorder on to future generations.

It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as genetic counselors or medical geneticists, who can provide appropriate guidance and support based on the results.

Test Name NUBPL Gene Leigh syndrome 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 NUBPL Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NUBPL Gene Leigh syndrome
Test Details

The NUBPL gene is associated with Leigh syndrome, a rare genetic disorder that affects the central nervous system. Leigh syndrome is characterized by progressive neurological deterioration, muscle weakness, movement disorders, and respiratory problems.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes, including the NUBPL gene. NGS can identify specific mutations or variations in the NUBPL gene that may be responsible for Leigh syndrome. This testing method provides a comprehensive analysis of the entire gene, increasing the chances of identifying potential disease-causing variants.

The NGS genetic test for the NUBPL gene can be used to confirm a diagnosis of Leigh syndrome, particularly in cases where the clinical presentation is consistent with the disorder. It can also be used for carrier testing, prenatal testing, or to assess the risk of passing the disorder on to future generations.

It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as genetic counselors or medical geneticists, who can provide appropriate guidance and support based on the results.

SKU: TEST-1492 Category:

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