NDUFS2 Gene Mitochondrial Complex I Deficiency Genetic Test
At DNA Labs UAE, we offer the NDUFS2 Gene Mitochondrial Complex I Deficiency Genetic Test. This test is designed to detect any deficiencies in the NDUFS2 gene, which is a subunit of the mitochondrial complex I enzyme. Mitochondrial complex I plays a crucial role in the electron transport chain, responsible for generating energy in the form of ATP within cells.
The NDUFS2 Gene Mitochondrial Complex I Deficiency Genetic Test is conducted using Next-Generation Sequencing (NGS) technology. This advanced sequencing method allows us to analyze multiple genes simultaneously, providing rapid and accurate results.
Test Details
The NDUFS2 Gene Mitochondrial Complex I Deficiency Genetic Test requires a DNA sample, which can be obtained through a blood sample or a cheek swab. The DNA sample is then sequenced using NGS technology to identify any mutations or variations in the NDUFS2 gene.
The test results, delivered within 3 to 4 weeks, can help diagnose NDUFS2 Gene Mitochondrial Complex I Deficiency and provide valuable information about the specific genetic changes causing the disorder.
Test Components and Price
- Test Name: NDUFS2 Gene Mitochondrial Complex I Deficiency Genetic Test
- Components: NGS Technology
- Price: 4400.0 AED
Sample Condition and Report Delivery
We accept blood samples, extracted DNA, or one drop of blood on an FTA card as sample conditions for the NDUFS2 Gene Mitochondrial Complex I Deficiency Genetic Test. The report will be delivered within 3 to 4 weeks.
Test Type and Doctor
The NDUFS2 Gene Mitochondrial Complex I Deficiency 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 NDUFS2 Gene Mitochondrial Complex I Deficiency Genetic Test is conducted by our Genetics department. Before the test, it is important to provide the clinical history of the patient and undergo a Genetic Counselling session to draw a pedigree chart of family members affected by NDUFS2 Gene Mitochondrial Complex I Deficiency.
Importance of Genetic Counseling and Professional Interpretation
It is crucial to note that NGS genetic testing is a complex procedure that should only be performed by trained professionals in a clinical genetics laboratory. We strongly recommend seeking genetic counseling and interpretation of the test results from a healthcare professional with expertise in genetics. This will ensure accurate diagnosis, appropriate treatment decisions, and comprehensive genetic counseling for affected individuals and their families.
| Test Name | NDUFS2 Gene Mitochondrial complex I deficiency 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 NDUFS2 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFS2 Gene Mitochondrial complex I deficiency |
| Test Details |
NDUFS2 gene mitochondrial complex I deficiency is a rare genetic disorder characterized by a deficiency in the NDUFS2 gene, which is a subunit of the mitochondrial complex I enzyme. Mitochondrial complex I is responsible for the first step in the electron transport chain, which is essential for generating energy in the form of adenosine triphosphate (ATP) within cells. A NGS genetic test, or Next-Generation Sequencing genetic test, is a type of genetic test that uses advanced sequencing technology to rapidly and accurately analyze multiple genes simultaneously. In the case of NDUFS2 gene mitochondrial complex I deficiency, an NGS genetic test can identify mutations or variations in the NDUFS2 gene that may be causing the deficiency. The NGS genetic test for NDUFS2 gene mitochondrial complex I deficiency involves obtaining a DNA sample from the individual, typically through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology to identify any mutations or variations in the NDUFS2 gene. The results of the NGS genetic test can help diagnose NDUFS2 gene mitochondrial complex I deficiency and provide information about the specific genetic changes that are causing the disorder. This information can be used to guide treatment decisions and provide genetic counseling to affected individuals and their families. It is important to note that NGS genetic testing is a complex and specialized procedure that should be performed by trained professionals in a clinical genetics laboratory. Genetic counseling and interpretation of the test results by a healthcare professional with expertise in genetics is also recommended. |
