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NDUFAF3 Gene Leigh syndrome Genetic Test

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

-21%

The NDUFAF3 gene Leigh syndrome genetic test is a specialized diagnostic procedure designed to detect mutations in the NDUFAF3 gene, which are associated with Leigh syndrome, a severe neurological disorder. This genetic condition typically manifests in infancy or early childhood and is characterized by progressive loss of mental and movement abilities. Symptoms may include developmental delay, muscle weakness, and breathing difficulties, among others. The test is crucial for early diagnosis and management of the syndrome, potentially guiding treatment options and genetic counseling.

Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, the test involves collecting a DNA sample from the patient, usually through a blood draw or cheek swab. The sample is then analyzed using sophisticated genetic sequencing technologies to identify any mutations in the NDUFAF3 gene that may indicate Leigh syndrome.

The cost of the NDUFAF3 gene Leigh syndrome genetic test at DNA Labs UAE is 4400 AED. While the price may seem high, the test provides invaluable information for affected families, helping them to understand the genetic basis of the condition, anticipate medical needs, and connect with supportive resources and communities. It’s important for potential patients to consult with a genetic counselor or healthcare provider to discuss the benefits, limitations, and implications of the test before proceeding.

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NDUFAF3 Gene Leigh Syndrome Genetic Test

Are you or a loved one experiencing symptoms of Leigh syndrome? DNA Labs UAE offers the NDUFAF3 Gene Leigh Syndrome Genetic Test to provide you with a comprehensive analysis of your genes and help guide treatment options.

Test Components and Price

The NDUFAF3 Gene Leigh Syndrome Genetic Test is priced at AED 4400.0. 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 to analyze multiple genes simultaneously.

Test Type and Doctor

The NDUFAF3 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 and Pre Test Information

The NDUFAF3 Gene Leigh Syndrome Genetic Test is conducted in the Genetics department. Prior to the test, it is important to provide the clinical history of the patient. A genetic counseling session may also be conducted to draw a pedigree chart of family members affected by NDUFAF3 Gene Leigh syndrome.

Understanding Leigh Syndrome and NGS Genetic Testing

Leigh syndrome is a rare genetic disorder that affects the central nervous system. It is characterized by progressive neurological deterioration, resulting in symptoms such as developmental delay, loss of motor skills, muscle weakness, and respiratory problems.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the case of Leigh syndrome, NGS can identify mutations or variations in the NDUFAF3 gene that may be causing the disorder. This comprehensive analysis allows for a more accurate diagnosis and can potentially guide treatment options.

Confirming the Presence of Mutations

If a person is suspected of having Leigh syndrome, NGS genetic testing can be recommended by a healthcare professional to confirm the presence of mutations in the NDUFAF3 gene. This information is crucial in understanding the cause of the disease and can provide valuable insights for genetic counseling and family planning.

Don’t wait any longer. Take control of your health and get tested for NDUFAF3 Gene Leigh Syndrome at DNA Labs UAE today.

Test Name NDUFAF3 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 NDUFAF3 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFAF3 Gene Leigh syndrome
Test Details

The NDUFAF3 gene is associated with Leigh syndrome, a rare genetic disorder that affects the central nervous system. Leigh syndrome is characterized by progressive neurological deterioration, which can lead to symptoms such as developmental delay, loss of motor skills, muscle weakness, and respiratory problems.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the case of Leigh syndrome, NGS can be used to identify mutations or variations in the NDUFAF3 gene that may be causing the disorder. This type of testing can provide a comprehensive analysis of the gene, allowing for a more accurate diagnosis and potentially guiding treatment options.

If a person is suspected of having Leigh syndrome, NGS genetic testing can be recommended by a healthcare professional to confirm the presence of mutations in the NDUFAF3 gene. This can help in understanding the cause of the disease and provide valuable information for genetic counseling and family planning.