GYS1 Gene Glycogen storage disease type 0 muscle Genetic Test
Welcome to DNA Labs UAE, where we offer the GYS1 Gene Glycogen storage disease type 0 muscle Genetic Test. This test is designed to identify any mutations or variations in the GYS1 gene that may be causing Glycogen Storage Disease Type 0 (GSD0), a rare genetic disorder that affects the storage and release of glycogen in the body.
Test Components
- 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: Metabolic Disorders
- Doctor: General Physician
- Test Department: Genetics
Pre Test Information
Prior to undergoing the GYS1 Gene Glycogen storage disease type 0 muscle 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 with Glycogen storage disease type 0 muscle.
Test Details
The GYS1 gene is associated with Glycogen Storage Disease Type 0 (GSD0), which primarily affects the muscles. Symptoms of GSD0 include muscle weakness, fatigue, and exercise intolerance. Our NGS (Next-Generation Sequencing) Genetic Test utilizes advanced sequencing technologies to analyze multiple genes simultaneously. In the case of GSD0, this test involves sequencing the GYS1 gene to identify any mutations or variations that may be causing the disease.
This genetic test is essential for diagnosing GSD0 and determining the specific genetic variant responsible for the disease in an individual. It can also be used for carrier testing in individuals with a family history of GSD0.
Please note that genetic testing should be conducted and interpreted by a qualified healthcare professional or genetic counselor. They can provide appropriate guidance and counseling based on the test results.
Test Name | GYS1 Gene Glycogen storage disease type 0 muscle Genetic Test |
---|---|
Components | |
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 | Metabolic Disorders |
Doctor | General Physician |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for GYS1 Gene Glycogen storage disease type 0 muscle NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Glycogen storage disease type 0 muscle |
Test Details |
The GYS1 gene is associated with Glycogen Storage Disease Type 0 (GSD0), a rare genetic disorder that affects the storage and release of glycogen in the body. GSD0 primarily affects the muscles, causing muscle weakness, fatigue, and exercise intolerance. NGS (Next-Generation Sequencing) Genetic Test refers to a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of GSD0, an NGS genetic test would involve sequencing the GYS1 gene to identify any mutations or variations that may be causing the disease. This genetic test can help diagnose GSD0 and determine the specific genetic variant causing the disease in an individual. It can also be used for carrier testing in individuals with a family history of GSD0. It is important to note that genetic testing should be conducted and interpreted by a qualified healthcare professional or genetic counselor, as they can provide appropriate guidance and counseling based on the results. |