MT-ND4 Gene Mitochondrial complex I deficiency Genetic Test
Genetic testing is an important tool in diagnosing and treating various disorders. One such disorder is MT-ND4 gene mitochondrial complex I deficiency, which affects the mitochondria, the energy-producing structures within cells.
Test Details
MT-ND4 gene mitochondrial complex I deficiency is caused by mutations in the MT-ND4 gene, which is responsible for producing a subunit of complex I, a crucial component of the mitochondrial respiratory chain. To diagnose this disorder, a genetic test called NGS (Next-Generation Sequencing) technology is used.
Components and Price
The cost of the MT-ND4 Gene Mitochondrial complex I deficiency Genetic Test is AED 4400.0. The test can be performed on a blood sample, extracted DNA, or even a drop of blood on an FTA Card.
Report Delivery
The report for the test is typically delivered within 3 to 4 weeks.
Test Type and Doctor
The MT-ND4 Gene Mitochondrial complex I deficiency Genetic Test falls under the category of Neurological Disorders. Therefore, it is recommended to consult with a Neurologist for this test.
Test Department
The test is conducted in the Genetics department of the laboratory.
Pre Test Information
Prior to the test, it is important to provide the clinical history of the patient who is undergoing the MT-ND4 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected with this disorder.
Test Procedure
The NGS genetic testing method involves obtaining a DNA sample, usually through a blood sample or cheek swab. The DNA is then sequenced using advanced sequencing technologies to identify any variations or mutations in the MT-ND4 gene.
Interpretation of Results
It is crucial to have the results of the test interpreted by a qualified healthcare provider who can provide appropriate counseling and guidance based on the individual’s specific genetic findings.
Overall, the MT-ND4 Gene Mitochondrial complex I deficiency Genetic Test is a valuable tool in diagnosing and managing this genetic disorder. By identifying mutations or variations in the MT-ND4 gene, healthcare professionals can better understand the condition and develop personalized treatment plans for patients.
| Test Name | MT-ND4 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 MT-ND4 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-ND4 Gene Mitochondrial complex I deficiency |
| Test Details |
MT-ND4 gene mitochondrial complex I deficiency is a genetic disorder that affects the mitochondria, the energy-producing structures within cells. This disorder is caused by mutations in the MT-ND4 gene, which is responsible for producing a subunit of complex I, a crucial component of the mitochondrial respiratory chain. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of MT-ND4 gene mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations or variations in the MT-ND4 gene that may be responsible for the disorder. The NGS genetic test involves obtaining a DNA sample, typically through a blood sample or cheek swab, and then sequencing the DNA to identify any variations or mutations in the MT-ND4 gene. The test can provide valuable information about the specific genetic changes present in an individual, which can aid in diagnosis and treatment planning. It is important to note that NGS genetic testing is typically performed by a healthcare professional or a specialized genetic testing laboratory. The results of the test should be interpreted by a qualified healthcare provider who can provide appropriate counseling and guidance based on the individual’s specific genetic findings. |
