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NDUFS3 Gene Leigh syndrome Genetic Test Cost

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

-21%

The NDUFS3 gene Leigh syndrome genetic test is a specialized diagnostic examination designed to identify mutations in the NDUFS3 gene, which are associated with Leigh syndrome. Leigh syndrome is a severe neurological disorder that typically emerges in infancy, characterized by progressive loss of mental and movement abilities. Mutations in the NDUFS3 gene disrupt the normal function of mitochondria, leading to the symptoms of the disorder.

This genetic test involves analyzing the patient’s DNA to detect mutations in the NDUFS3 gene that are known to cause Leigh syndrome. The process aids in the accurate diagnosis of the syndrome, enabling healthcare providers to tailor management and treatment plans according to the specific needs of the patient.

The test is available at DNA Labs UAE, a leading facility in genetic diagnostics, providing advanced genetic testing services. The cost of the NDUFS3 gene Leigh syndrome genetic test is 4400 AED. Conducting this test at DNA Labs UAE ensures that patients receive reliable results, thanks to the lab’s commitment to using cutting-edge technology and adhering to high standards of genetic analysis.

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NDUFS3 Gene Leigh Syndrome Genetic Test

At DNA Labs UAE, we offer the NDUFS3 Gene Leigh Syndrome Genetic Test for individuals who may be affected by Leigh syndrome, a rare and progressive neurological disorder. This test is designed to analyze the NDUFS3 gene, which is one of the genes associated with Leigh syndrome.

Test Components and Price

The NDUFS3 Gene Leigh Syndrome Genetic Test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery and Method

After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology, which allows for the analysis of multiple genes simultaneously.

Test Type and Doctor

The NDUFS3 Gene Leigh Syndrome Genetic Test falls under the category of neurological disorders. It is recommended to consult with a neurologist for this test.

Test Department

The test is conducted in our Genetics department, where our expert team specializes in genetic testing.

Pre Test Information

Before undergoing the NDUFS3 Gene Leigh Syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by NDUFS3 Gene Leigh Syndrome.

Test Details

Leigh syndrome is typically caused by mutations in genes involved in energy production within cells, including genes in the mitochondrial respiratory chain. The NDUFS3 gene is one of the genes associated with Leigh syndrome. NGS genetic testing allows for the analysis of the entire coding region of the NDUFS3 gene, identifying specific mutations or variants that may be associated with Leigh syndrome.

By undergoing the NDUFS3 Gene Leigh Syndrome Genetic Test, individuals can receive a definitive diagnosis, understand the underlying genetic cause of their condition, and potentially receive guidance on treatment options or genetic counseling.

It’s important to note that NGS genetic testing may not be available at all healthcare facilities and may require a referral to a specialized genetic testing laboratory. The interpretation of genetic test results should be done by a healthcare professional or genetic counselor who is knowledgeable about Leigh syndrome and genetic disorders.

Test Name NDUFS3 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 NDUFS3 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFS3 Gene Leigh syndrome
Test Details

The NDUFS3 gene is one of the genes associated with Leigh syndrome, a rare and progressive neurological disorder. Leigh syndrome is typically caused by mutations in genes involved in energy production within cells, including genes in the mitochondrial respiratory chain.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of Leigh syndrome, NGS genetic testing can be used to identify mutations in genes such as NDUFS3 that may be causing the condition.

By analyzing the entire coding region of the NDUFS3 gene, NGS testing can identify specific mutations or variants that may be associated with Leigh syndrome. This information can help in making a definitive diagnosis, understanding the underlying genetic cause, and potentially guiding treatment options or genetic counseling.

It’s important to note that NGS genetic testing may not be available at all healthcare facilities and may require a referral to a specialized genetic testing laboratory. Additionally, the interpretation of genetic test results should be done by a healthcare professional or genetic counselor who is knowledgeable about Leigh syndrome and genetic disorders.

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