Cori Disease, also known as glycogen storage disease type III, is a rare inherited disorder that affects the body's ability to break down glycogen into glucose. This debilitating condition can lead to various health complications, such as muscle weakness, enlarged liver, and low blood sugar levels. Synonyms for Cori Disease include Forbes Disease, Limit Dextrinosis, and Debrancher Deficiency. These alternative terms are used to describe the same genetic condition, which is caused by a missing or deficient enzyme called amylo-(1,6)-glucosidase. While there is currently no cure for Cori Disease, management options involve dietary modifications, regular medical check-ups, and monitoring of blood sugar levels to ensure optimal health and well-being.