SPEG Gene Centronuclear Myopathy Type 5 Genetic Test
At DNA Labs UAE, we offer the SPEG Gene Centronuclear Myopathy Type 5 Genetic Test at a cost of AED 4400.0. This test is used to diagnose and manage centronuclear myopathy type 5, a rare genetic disorder that affects muscle function.
Test Components
The SPEG Gene Centronuclear Myopathy Type 5 Genetic Test includes the following components:
- NGS Technology
- Neurological Disorders Test Type
- Genetics Test Department
Sample Condition
The test requires a sample of either blood, extracted DNA, or one drop of blood on an FTA card.
Report Delivery
Once the sample is received, the report will be delivered within 3 to 4 weeks.
Method
The test utilizes NGS (Next-Generation Sequencing) technology to analyze the SPEG gene.
Doctor and Test Department
The test is performed by a neurologist in our Genetics Test Department.
Pre Test Information
Before undergoing the SPEG Gene Centronuclear Myopathy Type 5 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 the disorder.
Test Details
The SPEG gene is associated with centronuclear myopathy type 5, a rare genetic disorder characterized by muscle weakness and wasting, particularly in the skeletal muscles. The NGS genetic test analyzes the SPEG gene to identify any mutations or variants that may be linked to the disorder.
This test is essential for diagnosing centronuclear myopathy type 5 and provides crucial information for managing the condition. It can also be used for carrier testing and family planning purposes.
Test Name | SPEG Gene Centronuclear 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 SPEG Gene Centronuclear myopathy type 5 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SPEG Gene Centronuclear myopathy type 5 |
Test Details |
The SPEG gene is associated with centronuclear myopathy type 5, a rare genetic disorder that affects muscle function. The disorder is characterized by muscle weakness and wasting, particularly in the skeletal muscles. The NGS genetic test is a type of genetic testing that uses next-generation sequencing technology to analyze the SPEG gene and identify any mutations or variants that may be associated with centronuclear myopathy type 5. This test can help diagnose the disorder and provide important information for managing the condition. It may also be used for carrier testing and family planning purposes. |