Explore this section to learn more about Type I Glycogen Storage Disease, including a description of the disease and how it's diagnosed.
Glycogen storage disease type I (also known as GSDI or von Gierke disease) is an inherited disorder caused by the buildup of a complex sugar called ...
Prevalence. Overall, according to a study in British Columbia, approximately 2.3 children per 100 000 births (1 in 43,000) have some form of glycogen storage disease. 
Glycogen storage disease (GSD) type I is also known as von Gierke disease or hepatorenal glycogenosis. von Gierke  described the first patient with GSD ...
Information about glycogen storage disease (GSD) types, causes, symptoms, diagnosis, treatment and outlook, provided by Cincinnati Children's.
Glycogen storage diseases information including symptoms, diagnosis, misdiagnosis, ... Glycogen storage disease type II can affect both the liver and heart.
What Is Glycogen Storage Disease? Glycogen storage diseases (GSDs) are a group of inherited genetic disorders that cause glycogen to be improperly stored in the body.
The Association for Glycogen Storage Disease - AGSD - was established in 1979 in order to create an organization which would be a focus for parents of and individuals ...
Glycogen Storage Diseases Definition Glycogen serves as the primary fuel reserve for the body's energy needs. Glycogen storage diseases, also known as glycogenoses ...
Clinical characteristics. Glycogen storage disease type I (GSDI) is characterized by accumulation of glycogen and fat in the liver and kidneys, resulting in ...