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Accurate Test Results for AGL Gene Glycogen storage disease type 3 NGS Genetic DNA Test
AGL Gene Glycogen storage disease type 3 NGS Genetic DNA Test Cost 20000 Rs
AGL Gene Glycogen storage disease type 3 NGS Genetic DNA Test Details
AGL Gene Glycogen Storage Disease Type 3 NGS Genetic DNA Test
Glycogen storage disease type 3, also known as Cori disease, is a rare genetic disorder that affects the body's ability to break down glycogen, a complex sugar that is stored in the liver and muscle tissues. This condition is caused by mutations in the AGL gene, which provides instructions for making an enzyme called glycogen debranching enzyme (GDE).
People with glycogen storage disease type 3 have a deficiency of GDE, which leads to an accumulation of abnormal glycogen in their liver and muscle cells. This can cause a wide range of symptoms, including:
- Enlarged liver (hepatomegaly)
- Low blood sugar (hypoglycemia)
- Muscle weakness and wasting
- Delayed growth and development
- Cardiomyopathy
If left untreated, glycogen storage disease type 3 can lead to liver and heart damage, as well as other serious health complications.
Diagnosis of Glycogen Storage Disease Type 3
Diagnosing glycogen storage disease type 3 typically involves a combination of clinical evaluation, blood tests, and genetic testing. Blood tests can help to measure the levels of certain enzymes and metabolites in the blood, which can be indicative of the disease. Genetic testing, such as Next-Generation Sequencing (NGS), can identify mutations in the AGL gene that are responsible for the condition.
NGS Genetic DNA Test for Glycogen Storage Disease Type 3
NGS is a powerful genetic testing technology that allows for the rapid sequencing of large sections of DNA. This type of testing can identify mutations in the AGL gene that are responsible for glycogen storage disease type 3 with high accuracy.
The cost of an NGS genetic DNA test for glycogen storage disease type 3 in India is typically around INR 20,000. This cost may vary depending on the specific testing facility and any additional fees for consultation or interpretation of the results.
Conclusion
Glycogen storage disease type 3 is a rare genetic disorder that can cause a range of symptoms, including liver and muscle damage, low blood sugar, and delayed growth and development. NGS genetic DNA testing can help to identify mutations in the AGL gene that are responsible for the condition, allowing for early diagnosis and treatment. If you or someone you know is experiencing symptoms of glycogen storage disease type 3, it is important to speak with a healthcare professional as soon as possible.
For reliable and accurate NGS genetic DNA testing in India, DNA Labs India is the leading provider of genetic testing services. Our state-of-the-art laboratory facilities and expert team of geneticists ensure that you receive the highest quality genetic testing services at an affordable cost. Contact us today to learn more about our genetic testing services and how we can help you.
