NDUFB3 Gene Mitochondrial Complex I Deficiency Genetic Test
Welcome to the DNA Labs UAE blog, where we provide valuable information about genetic testing. In this article, we will discuss the NDUFB3 Gene Mitochondrial Complex I Deficiency Genetic Test.
Test Components and Price
The NDUFB3 Gene Mitochondrial Complex I Deficiency 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
The report for the NDUFB3 Gene Mitochondrial Complex I Deficiency Genetic Test 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 NDUFB3 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 NDUFB3 Gene Mitochondrial Complex I Deficiency Genetic Test is conducted by our Genetics department. Before undergoing the test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be arranged to draw a pedigree chart of family members affected by NDUFB3 Gene Mitochondrial Complex I Deficiency.
Test Details
The NDUFB3 gene encodes a subunit of mitochondrial complex I, which plays a crucial role in oxidative phosphorylation in mitochondria. Mitochondrial complex I deficiency refers to a group of genetic disorders caused by mutations in genes that encode subunits of complex I, including the NDUFB3 gene.
NGS genetic testing, using advanced sequencing technologies, can analyze the entire coding region of the NDUFB3 gene. This test helps identify both common and rare mutations associated with mitochondrial complex I deficiency, aiding in diagnosis, disease progression prediction, and treatment decisions.
It is important to note that NGS genetic testing may not identify all possible mutations, as there may be variations in non-coding regions of the gene or other genes contributing to the condition. Therefore, additional testing methods such as targeted gene sequencing or whole exome sequencing may be necessary to further investigate the genetic cause of mitochondrial complex I deficiency.
Thank you for reading our blog post about the NDUFB3 Gene Mitochondrial Complex I Deficiency Genetic Test. For more information or to schedule a test, please contact DNA Labs UAE.
| Test Name | NDUFB3 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 NDUFB3 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFB3 Gene Mitochondrial complex I deficiency |
| Test Details | The NDUFB3 gene is a gene that encodes a subunit of mitochondrial complex I, which is one of the five protein complexes involved in oxidative phosphorylation in mitochondria. Mitochondrial complex I deficiency refers to a group of genetic disorders that result from mutations in genes encoding subunits of complex I, including the NDUFB3 gene. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations in genes such as NDUFB3 that may be responsible for the condition. By analyzing the entire coding region of the NDUFB3 gene, NGS genetic testing can detect both common and rare mutations that may be associated with mitochondrial complex I deficiency. This information can be helpful in confirming a diagnosis, predicting disease progression, and guiding treatment decisions. It is important to note that NGS genetic testing may not identify all possible mutations, as there may be variations in the non-coding regions of the gene or in other genes that contribute to the condition. Therefore, additional testing methods, such as targeted gene sequencing or whole exome sequencing, may be necessary to further investigate the genetic cause of mitochondrial complex I deficiency. |
