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SURF1 Gene Leigh syndrome due to COX deficiency Genetic Test

3,200 د.إ

-43%

The “SURF1 Gene Leigh Syndrome due to COX Deficiency Genetic Test” is a specialized diagnostic tool offered by DNA Labs UAE, aimed at detecting mutations in the SURF1 gene. These mutations are known to cause Leigh Syndrome, a severe neurological disorder that typically emerges in the first year of life. Leigh Syndrome associated with cytochrome c oxidase (COX) deficiency is specifically linked to the SURF1 gene alterations. This condition leads to progressive loss of mental and movement abilities, which can be fatal. The test, which costs 3200 AED, is crucial for early diagnosis and management of the syndrome. It involves analyzing the patient’s DNA to identify any mutations in the SURF1 gene, providing vital information for treatment planning and genetic counseling for affected families. Conducted in the advanced facilities of DNA Labs UAE, this test is a key step towards personalized medicine for patients with Leigh Syndrome due to COX deficiency.

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SURF1 Gene Leigh Syndrome due to COX Deficiency Genetic Test

At DNA Labs UAE, we offer the SURF1 Gene Leigh syndrome due to COX deficiency genetic test. This test helps in the diagnosis of Leigh syndrome, a severe neurological disorder associated with the SURF1 gene.

Test Components and Price

The test is priced at 3200.0 AED. The sample condition required for testing includes blood, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

The test results are typically delivered within 3 to 4 weeks.

Method

The SURF1 Gene Leigh syndrome due to COX deficiency genetic test utilizes NGS (Next-Generation Sequencing) technology.

Test Type and Doctor

This test is specifically designed for the diagnosis of neurological disorders and is performed by a neurologist.

Test Department

The test is conducted in our Genetics department.

Pre-Test Information

Prior to the test, it is important to provide the clinical history of the patient who is undergoing the SURF1 Gene Leigh syndrome due to COX deficiency NGS genetic DNA test. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by SURF1 Gene Leigh syndrome due to COX deficiency.

Test Details

The SURF1 gene is associated with Leigh syndrome due to COX deficiency, a severe neurological disorder. Mutations in the SURF1 gene lead to a deficiency in the cytochrome c oxidase (COX) enzyme, which is involved in cellular respiration. The NGS genetic testing method allows for the analysis of the SURF1 gene, identifying any mutations or variants that may be present. This comprehensive testing approach provides valuable information about the patient’s genetic makeup.

Importance of Genetic Testing

Genetic testing for Leigh syndrome due to COX deficiency can confirm a diagnosis, provide a prognosis, and offer potential treatment options. It can also be used for carrier testing in individuals with a family history of the condition or for prenatal testing in couples at risk of having a child with the disorder. Additionally, genetic testing can assist with genetic counseling and family planning decisions.

Test Name SURF1 Gene Leigh syndrome due to COX deficiency Genetic Test
Components
Price 3200.0 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 SURF1 Gene Leigh syndrome due to COX deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SURF1 Gene Leigh syndrome due to COX deficiency
Test Details

The SURF1 gene is associated with a form of Leigh syndrome, a severe neurological disorder. Leigh syndrome due to COX deficiency is caused by mutations in the SURF1 gene, leading to a deficiency in the cytochrome c oxidase (COX) enzyme, which is involved in cellular respiration.

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the SURF1 gene and identify any mutations or variants that may be present. This type of testing allows for the simultaneous analysis of multiple genes, providing a comprehensive view of the patient’s genetic makeup.

By identifying mutations in the SURF1 gene, NGS genetic testing can help confirm a diagnosis of Leigh syndrome due to COX deficiency. It can also be used for carrier testing in individuals with a family history of the condition or for prenatal testing in couples at risk of having a child with the disorder.

Genetic testing can provide valuable information for patients and their families, including a definitive diagnosis, prognosis, and potential treatment options. It can also help with genetic counseling and family planning decisions.