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NDUFAF2 Gene Leigh syndrome Genetic Test

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

-21%

The NDUFAF2 Gene Leigh Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the NDUFAF2 gene, which are linked to Leigh syndrome. Leigh syndrome is a severe neurological disorder that typically emerges in the first year of life, characterized by progressive loss of mental and movement abilities. The condition can result from genetic mutations affecting the mitochondrial function, with the NDUFAF2 gene playing a crucial role in mitochondrial complex I assembly.

This genetic test is vital for early detection and management of Leigh syndrome, allowing for a better understanding of the condition and aiding in the development of a tailored treatment plan for affected individuals. By analyzing the patient’s DNA, the test can confirm the presence of mutations in the NDUFAF2 gene, providing essential information for families and healthcare providers.

The cost of the NDUFAF2 Gene Leigh Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the sophisticated genetic analysis required to pinpoint the specific mutations associated with the disorder. Given the complexity and the specialized nature of this test, it represents a critical step forward in the care and management of patients potentially suffering from Leigh syndrome, offering hope and direction for affected families.

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NDUFAF2 Gene Leigh Syndrome Genetic Test

Test Name: NDUFAF2 Gene Leigh Syndrome Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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 NDUFAF2 Gene Leigh Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFAF2 Gene Leigh Syndrome.

Test Details

The NDUFAF2 gene is associated with Leigh syndrome, a rare genetic disorder that affects the central nervous system. Leigh syndrome is characterized by progressive neurological deterioration, including muscle weakness, movement disorders, seizures, and respiratory problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the NDUFAF2 gene. NGS testing can identify specific mutations or changes in the NDUFAF2 gene that may be responsible for Leigh syndrome.

By identifying the specific genetic mutation causing Leigh syndrome in an individual, NGS testing can provide a definitive diagnosis, guide treatment decisions, and inform genetic counseling for the affected individual and their family members. It can also help in identifying potential carriers of the genetic mutation.

It is important to note that NGS testing for Leigh syndrome should be conducted by a qualified geneticist or genetic counselor, as the interpretation of the test results can be complex and requires expertise in genetics. Additionally, NGS testing may not be available in all healthcare settings and may have associated costs and insurance coverage considerations.

Test Name NDUFAF2 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 NDUFAF2 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFAF2 Gene Leigh syndrome
Test Details

The NDUFAF2 gene is associated with Leigh syndrome, a rare genetic disorder that affects the central nervous system. Leigh syndrome is characterized by progressive neurological deterioration, including muscle weakness, movement disorders, seizures, and respiratory problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the NDUFAF2 gene. NGS testing can identify specific mutations or changes in the NDUFAF2 gene that may be responsible for Leigh syndrome.

By identifying the specific genetic mutation causing Leigh syndrome in an individual, NGS testing can provide a definitive diagnosis, guide treatment decisions, and inform genetic counseling for the affected individual and their family members. It can also help in identifying potential carriers of the genetic mutation.

It is important to note that NGS testing for Leigh syndrome should be conducted by a qualified geneticist or genetic counselor, as the interpretation of the test results can be complex and requires expertise in genetics. Additionally, NGS testing may not be available in all healthcare settings and may have associated costs and insurance coverage considerations.