MTMR14 Gene Centronuclear Myopathy Type 1 Genetic Test
Are you or your family members experiencing symptoms of centronuclear myopathy type 1? DNA Labs UAE offers the MTMR14 Gene Centronuclear Myopathy Type 1 Genetic Test to help diagnose and provide valuable information about this rare genetic disorder.
Test Details
The MTMR14 Gene Centronuclear Myopathy Type 1 NGS genetic test is a type of genetic testing that detects mutations or changes in the MTMR14 gene associated with centronuclear myopathy type 1. This test utilizes next-generation sequencing (NGS) technology, allowing for the simultaneous analysis of multiple genes in a single test.
Centronuclear Myopathy Type 1
Centronuclear myopathy type 1 is a rare genetic disorder that affects the muscles, leading to muscle weakness and wasting. It is caused by mutations in the MTMR14 gene, which produces a protein called myotubularin-related protein 14. This protein plays a crucial role in the normal function of muscle cells.
Test Process
The MTMR14 Gene Centronuclear Myopathy Type 1 NGS genetic test requires a blood or extracted DNA sample. Alternatively, one drop of blood on an FTA card can also be used. Once the sample is collected, it is sent to our laboratory for analysis. The results are typically delivered within 3 to 4 weeks.
Why Should You Get Tested?
If you or your family members are experiencing symptoms of centronuclear myopathy type 1 or have a family history of the condition, this genetic test can help confirm a diagnosis and provide valuable information about the genetic cause of the disorder. This information can guide treatment and management strategies and enable genetic counseling for affected individuals and their families.
Pre-Test Information
Prior to undergoing the MTMR14 Gene Centronuclear Myopathy Type 1 NGS genetic test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by centronuclear myopathy type 1.
Test Cost and Doctor
The cost of the MTMR14 Gene Centronuclear Myopathy Type 1 Genetic Test is AED 4400.0. This test is typically ordered by a neurologist, specializing in neurological disorders. Our test department focuses on genetics, ensuring accurate and reliable results.
Make an Appointment
If you suspect centronuclear myopathy type 1 or require further information about the MTMR14 Gene Centronuclear Myopathy Type 1 Genetic Test, please schedule an appointment with our experienced healthcare providers. They will guide you through the process and help you understand the results.
| Test Name | MTMR14 Gene Centronuclear myopathy type 1 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 MTMR14 Gene Centronuclear myopathy type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MTMR14 Gene Centronuclear myopathy type 1 |
| Test Details |
MTMR14 gene centronuclear myopathy type 1 NGS genetic test is a type of genetic testing that is used to detect mutations or changes in the MTMR14 gene that are associated with centronuclear myopathy type 1. This test is done using next-generation sequencing (NGS) technology, which allows for the simultaneous analysis of multiple genes in a single test. Centronuclear myopathy type 1 is a rare genetic disorder that affects the muscles and causes muscle weakness and wasting. It is caused by mutations in the MTMR14 gene, which provides instructions for making a protein called myotubularin-related protein 14. This protein is important for the normal function of muscle cells. The MTMR14 gene centronuclear myopathy type 1 NGS genetic test is typically ordered for individuals who have symptoms of centronuclear myopathy type 1 or who have a family history of the condition. The test can help confirm a diagnosis and provide information about the genetic cause of the condition. This information can be used to guide treatment and management strategies and to provide genetic counseling to affected individuals and their families. The MTMR14 gene centronuclear myopathy type 1 NGS genetic test is performed on a blood sample or a saliva sample. The sample is sent to a laboratory for analysis, and the results are typically available within a few weeks. The test is usually ordered by a healthcare provider, such as a genetic counselor or a physician who specializes in neuromuscular disorders. |
