TNNT1 Gene Nemaline myopathy type 5 Genetic Test
Components: TNNT1 Gene Nemaline myopathy type 5 Genetic Test
Price: 4400.0 AED
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
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 TNNT1 Gene Nemaline myopathy type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TNNT1 Gene Nemaline myopathy type 5.
Test Details
The TNNT1 gene is associated with nemaline myopathy type 5, a rare genetic disorder characterized by muscle weakness and respiratory problems. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the identification of genetic variations or mutations that may be responsible for the condition.
By sequencing the TNNT1 gene, NGS testing can help confirm a diagnosis of nemaline myopathy type 5 and provide information about the specific genetic variant involved. This information can be useful for genetic counseling, determining disease prognosis, and potentially guiding treatment decisions.
Test Name | TNNT1 Gene Nemaline myopathy type 5 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 TNNT1 Gene Nemaline myopathy type 5 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TNNT1 Gene Nemaline myopathy type 5 |
Test Details |
The TNNT1 gene is associated with nemaline myopathy type 5, a rare genetic disorder characterized by muscle weakness and respiratory problems. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the identification of genetic variations or mutations that may be responsible for the condition. By sequencing the TNNT1 gene, NGS testing can help confirm a diagnosis of nemaline myopathy type 5 and provide information about the specific genetic variant involved. This information can be useful for genetic counseling, determining disease prognosis, and potentially guiding treatment decisions. |