Glycogen storage diseases (GSDs) are a group of inherited disorders characterized by deficiencies in the enzymes responsible for glycogen synthesis or breakdown. These deficiencies can result in abnormal glycogen accumulation or inadequate glucose production. While primarily genetic, some environmental factors, such as exposure to certain toxins, can exacerbate these conditions. Understanding these diseases is important in toxicology for the identification of potential environmental triggers and the management of health risks in vulnerable populations.
