Other Glycogen Storage Disease (OGSD) is a rare genetic disorder that affects the storage and release of glycogen in the body. Glycogen is a complex carbohydrate that serves as a primary source of energy in the body. In people with OGSD, the body is unable to store or release glycogen properly, which can lead to a variety of health problems.
There are several types of OGSD, each of which is caused by a different genetic mutation. These include:
The symptoms of OGSD can vary depending on the type of disorder and the severity of the condition. Some common symptoms include:
Diagnosis of OGSD involves a combination of physical exam, medical history, and laboratory tests. Blood tests can be used to measure glycogen levels in the body, as well as to identify any genetic mutations that may be causing the disorder.
OGSD is a rare genetic disorder that affects the storage and release of glycogen in the body. There are several different types of OGSD, each of which is caused by a different genetic mutation. The symptoms of OGSD can vary depending on the type of disorder and the severity of
Glycogen storage diseases (GSDs) are a group of inherited metabolic disorders that affect how the body stores and uses glycogen. There are several types of GSDs, including other glycogen storage diseases, which are less common than the more well-known types like Pompe disease and Von Gierke disease.
Other glycogen storag...
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