Glycogen storage disease type 3 (GSD III), also known as Cori’s disease or Forbes’ disease, is a rare genetic disorder that affects the body’s ability to break down glycogen. This condition is caused by mutations in the AGL gene, which leads to the accumulation of abnormal glycogen in tissues, particularly in the liver and muscles, causing various health issues. At DNA Labs UAE, we offer a comprehensive genetic test for those concerned about this condition, with detailed insights into the symptoms and necessary steps for diagnosis and management.
Understanding Glycogen Storage Disease Type 3
Glycogen Storage Disease Type 3 is an inherited metabolic disorder that disrupts the normal processing of glycogen, a complex sugar molecule that serves as a primary energy source. The AGL gene provides instructions for making an enzyme necessary for breaking down glycogen. Mutations in this gene result in the production of an abnormal enzyme that cannot effectively break down glycogen, leading to its accumulation in the body.
Symptoms of Glycogen Storage Disease Type 3
The symptoms of GSD III vary among affected individuals and largely depend on the organs involved. The most common symptoms include:
- Low blood sugar (hypoglycemia)
- Muscle weakness
- Enlarged liver (hepatomegaly)
- Delayed growth or short stature
- Increased levels of fats in the blood (hyperlipidemia)
- Increased levels of liver enzymes in the blood
Individuals with GSD III may also experience progressive muscle wasting (myopathy), leading to difficulties in physical activities and in severe cases, respiratory problems. It’s crucial for those experiencing these symptoms to seek a genetic test for a definitive diagnosis.
AGL Gene Glycogen Storage Disease Type 3 Genetic Test at DNA Labs UAE
At DNA Labs UAE, we understand the importance of accurate diagnosis and effective management of Glycogen Storage Disease Type 3. Our AGL gene glycogen storage disease type 3 genetic test is designed to identify mutations in the AGL gene, providing crucial information for individuals and families affected by this condition. The test is priced at 4400 AED, reflecting our commitment to offering high-quality, accessible genetic testing services.
To learn more about this test and to schedule your appointment, please visit our website at DNA Labs UAE.
Why Choose DNA Labs UAE for Your Genetic Testing Needs?
DNA Labs UAE is at the forefront of genetic testing services in the United Arab Emirates. Our state-of-the-art facilities and highly qualified team of geneticists and medical professionals ensure the highest accuracy and reliability of test results. We are committed to providing personalized care and support throughout the testing process, helping our clients understand their results and the implications for their health and lifestyle.
Conclusion
Glycogen Storage Disease Type 3 is a rare but impactful condition that requires careful management and monitoring. Understanding the symptoms and undergoing genetic testing can provide valuable insights for affected individuals and their families. DNA Labs UAE is here to support you with comprehensive testing services, expert guidance, and compassionate care. If you suspect you or a loved one may be affected by GSD III, we encourage you to reach out to us and take the first step towards clarity and peace of mind.
