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NDUFA2 Gene Leigh syndrome Genetic Test

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

-21%

The NDUFA2 gene test for Leigh syndrome is a specialized genetic examination offered by DNA Labs UAE, aimed at diagnosing this rare and severe neurological disorder. Leigh syndrome, also known as Leigh’s disease, is a progressive condition that typically emerges in infancy or early childhood, affecting the central nervous system and leading to a wide array of symptoms, including motor and developmental delays, breathing difficulties, and seizures. The condition is linked to mutations in various genes, including NDUFA2, which plays a critical role in the mitochondrial function and energy production within cells.

The test involves analyzing the patient’s DNA to identify mutations in the NDUFA2 gene that are associated with Leigh syndrome. This precise genetic testing can provide essential information for diagnosing the condition, understanding its progression, and guiding treatment options. It is particularly valuable for families with a history of Leigh syndrome or related mitochondrial disorders, offering insights that can aid in early intervention and management strategies.

Conducted at DNA Labs UAE, a facility renowned for its state-of-the-art technology and expertise in genetic diagnostics, the NDUFA2 gene test for Leigh syndrome is priced at 4400 AED. This cost reflects the comprehensive nature of the test, from the initial DNA extraction to the detailed analysis and reporting of results. For families facing the possibility of Leigh syndrome, this test represents a critical step towards obtaining a definitive diagnosis and accessing the necessary support and treatments to manage the condition.

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NDUFA2 Gene Leigh Syndrome Genetic Test

Components: NDUFA2 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 NDUFA2 Gene Leigh syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFA2 Gene Leigh syndrome.

Test Details

The NDUFA2 gene is associated with Leigh syndrome, which is a rare genetic disorder that affects the central nervous system. Leigh syndrome is characterized by progressive neurological deterioration, which can include symptoms such as developmental delays, muscle weakness, movement disorders, and respiratory problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously. In the case of Leigh syndrome, NGS genetic testing can be used to identify mutations or variations in the NDUFA2 gene that may be responsible for the disorder. By analyzing the NDUFA2 gene using NGS technology, healthcare professionals can identify specific genetic changes that may be causing Leigh syndrome in an individual.

This information can be helpful in diagnosing the condition, understanding its progression, and providing appropriate treatment and management strategies. It’s important to note that genetic testing for Leigh syndrome and other genetic disorders should be conducted by healthcare professionals with expertise in genetics. They can provide appropriate counseling and guidance based on the results of the genetic test.

Test Name NDUFA2 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 NDUFA2 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFA2 Gene Leigh syndrome
Test Details

The NDUFA2 gene is associated with Leigh syndrome, which is a rare genetic disorder that affects the central nervous system. Leigh syndrome is characterized by progressive neurological deterioration, which can include symptoms such as developmental delays, muscle weakness, movement disorders, and respiratory problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously. In the case of Leigh syndrome, NGS genetic testing can be used to identify mutations or variations in the NDUFA2 gene that may be responsible for the disorder.

By analyzing the NDUFA2 gene using NGS technology, healthcare professionals can identify specific genetic changes that may be causing Leigh syndrome in an individual. This information can be helpful in diagnosing the condition, understanding its progression, and providing appropriate treatment and management strategies.

It’s important to note that genetic testing for Leigh syndrome and other genetic disorders should be conducted by healthcare professionals with expertise in genetics. They can provide appropriate counseling and guidance based on the results of the genetic test.