MT-TW Gene Encephalopathy mitochondrial MT-TW related Genetic Test
Genetic testing is an important tool in diagnosing and understanding genetic disorders. One such disorder is MT-TW gene encephalopathy mitochondrial, which affects the function of mitochondria, the energy-producing structures in cells.
This rare genetic disorder is caused by mutations in the MT-TW gene, which provides instructions for making a specific mitochondrial transfer RNA molecule. The MT-TW gene is located in the mitochondrial DNA and is inherited maternally.
At DNA Labs UAE, we offer a comprehensive MT-TW gene encephalopathy mitochondrial MT-TW related genetic test. This test utilizes Next-Generation Sequencing (NGS) technology, which allows for the simultaneous analysis of multiple genes.
The MT-TW related NGS genetic test involves obtaining a sample of DNA, typically from a blood sample. Our team of experts will then analyze the sample using NGS technology to detect mutations in the MT-TW gene that are associated with encephalopathy mitochondrial.
Our MT-TW gene encephalopathy mitochondrial MT-TW related genetic test is performed in our Genetics department by our experienced Neurologist. The test is specifically designed for individuals with neurological disorders.
The cost of the MT-TW gene encephalopathy mitochondrial MT-TW related genetic test is 4400.0 AED. We accept samples in the form of blood or extracted DNA, or even one drop of blood on an FTA card.
Once the sample is received, the report delivery time is typically 3 to 4 weeks. During this time, our team will thoroughly analyze the sample and provide a detailed report.
Prior to the test, it is important to provide us with the clinical history of the patient who is going for the MT-TW gene encephalopathy mitochondrial MT-TW related NGS genetic DNA test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with the disorder.
By undergoing the MT-TW gene encephalopathy mitochondrial MT-TW related genetic test, individuals can confirm a diagnosis, make informed treatment decisions, and gain insight into the risk of passing the condition on to future generations.
Test Name | MT-TW Gene Encephalopathy mitochondrial MT-TW related Genetic Test |
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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-TW Gene Encephalopathy mitochondrial, MT-TW related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-TW Gene Encephalopathy mitochondrial, MT-TW related |
Test Details |
MT-TW gene encephalopathy mitochondrial is a rare genetic disorder that affects the function of the mitochondria, the energy-producing structures in cells. This disorder is caused by mutations in the MT-TW gene, which provides instructions for making a specific mitochondrial transfer RNA molecule. The MT-TW gene is located in the mitochondrial DNA, which is inherited maternally. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced technology to analyze multiple genes simultaneously. NGS can be used to identify mutations in the MT-TW gene that cause encephalopathy mitochondrial. The MT-TW related NGS genetic test involves obtaining a sample of DNA, typically from a blood sample, and analyzing it using NGS technology. The test can detect mutations in the MT-TW gene that are associated with encephalopathy mitochondrial. This information can be used to confirm a diagnosis, inform treatment decisions, and provide information about the risk of passing the condition on to future generations. |