MYOT Gene Myotilinopathy Genetic Test
Components: MYOT Gene Myotilinopathy 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 MYOT Gene Myotilinopathy NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MYOT Gene Myotilinopathy
Test Details
The MYOT gene, also known as myotilin, is responsible for producing a protein called myotilin. Mutations in this gene can lead to a condition called myotilinopathy, which is a type of muscular dystrophy.
To diagnose myotilinopathy, a Next-Generation Sequencing (NGS) genetic test can be performed. This test involves sequencing the DNA of an individual to identify any mutations or changes in the MYOT gene that may be causing the condition.
NGS allows for the analysis of multiple genes simultaneously, making it a more efficient and cost-effective method compared to traditional sequencing techniques.
NGS genetic testing can provide valuable information about the specific genetic mutations present in an individual’s MYOT gene, helping to confirm a diagnosis of myotilinopathy. It can also provide information about the inheritance pattern of the condition, which can be useful for family planning and genetic counseling.
It’s important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor, who can help interpret the results and provide appropriate recommendations and support.
| Test Name | MYOT Gene Myotilinopathy 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 MYOT Gene Myotilinopathy NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MYOT Gene Myotilinopathy |
| Test Details |
The MYOT gene, also known as myotilin, is responsible for producing a protein called myotilin. Mutations in this gene can lead to a condition called myotilinopathy, which is a type of muscular dystrophy. To diagnose myotilinopathy, a Next-Generation Sequencing (NGS) genetic test can be performed. This test involves sequencing the DNA of an individual to identify any mutations or changes in the MYOT gene that may be causing the condition. NGS allows for the analysis of multiple genes simultaneously, making it a more efficient and cost-effective method compared to traditional sequencing techniques. NGS genetic testing can provide valuable information about the specific genetic mutations present in an individual’s MYOT gene, helping to confirm a diagnosis of myotilinopathy. It can also provide information about the inheritance pattern of the condition, which can be useful for family planning and genetic counseling. It’s important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor, who can help interpret the results and provide appropriate recommendations and support. |
