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NDUFS8 Gene Leigh syndrome Genetic Test Cost

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

-21%

The NDUFS8 gene Leigh syndrome genetic test is a specialized diagnostic tool available at DNA Labs UAE, designed to detect mutations in the NDUFS8 gene that are associated with Leigh syndrome, a severe neurological disorder. This genetic condition typically manifests in infancy or early childhood and can lead to progressive loss of mental and movement abilities, ultimately resulting in serious health complications. The test is particularly crucial for early detection and management of the syndrome, offering families and healthcare providers vital information for planning treatment and care strategies. Priced at 4400 AED, the test involves analyzing the patient’s DNA to identify any genetic alterations in the NDUFS8 gene, providing a clear diagnosis and helping to guide potential therapeutic interventions. DNA Labs UAE employs advanced genetic testing technologies to ensure accurate and reliable results, supporting patients and their families in navigating the complexities of genetic disorders like Leigh syndrome.

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NDUFS8 Gene Leigh Syndrome Genetic Test

Welcome to DNA Labs UAE, where we offer the NDUFS8 Gene Leigh Syndrome Genetic Test. This test is designed to diagnose and provide valuable information about Leigh syndrome, a rare genetic disorder that affects the central nervous system.

Test Components and Price

Test Name: NDUFS8 Gene Leigh Syndrome Genetic Test

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

Price: 4400.0 AED

Sample Condition

We accept blood samples, extracted DNA samples, or one drop of blood on FTA Card for this test.

Report Delivery

After the sample is received, the report will be delivered within 3 to 4 weeks.

Test Method

We use NGS (Next-Generation Sequencing) technology for this genetic test. NGS allows us to analyze multiple genes simultaneously, providing accurate and comprehensive results.

Test Type and Department

Test Type: Neurological Disorders

Test Department: Genetics

Referring Doctor

Doctor: Neurologist

Pre Test Information

Before undergoing the NDUFS8 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 NDUFS8 Gene Leigh Syndrome.

Test Details

The NDUFS8 gene is associated with Leigh syndrome, a rare genetic disorder characterized by progressive neurological deterioration. Symptoms include loss of motor skills, muscle weakness, seizures, and respiratory problems. NGS genetic testing allows us to identify mutations or variations in the NDUFS8 gene that may be causing the disorder. This information is crucial for an accurate diagnosis, understanding the underlying cause, and potentially guiding treatment decisions.

Please note that NGS genetic testing for Leigh syndrome may not be available in all healthcare settings. It is recommended to consult with a healthcare provider or genetic counselor for more information about the availability and appropriateness of this test for an individual.

Test Name NDUFS8 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 NDUFS8 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFS8 Gene Leigh syndrome
Test Details

The NDUFS8 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, including loss of motor skills, muscle weakness, seizures, and respiratory problems.

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 or variations in the NDUFS8 gene that may be causing the disorder.

By analyzing the NDUFS8 gene, NGS genetic testing can provide valuable information about the specific genetic changes that are contributing to Leigh syndrome in an individual. This information can help in making an accurate diagnosis, understanding the underlying cause of the disorder, and potentially guiding treatment decisions.

It is important to note that NGS genetic testing for Leigh syndrome may not be available in all healthcare settings. A healthcare provider or genetic counselor can provide more information about the availability and appropriateness of this test for an individual.

SKU: TEST-1491 Category:

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