Cori Disease (Type III)
Cori Disease, also called glycogen storage disease type III (GSD-III) or Forbes disease, is an autosomal recessive lysosomal storage disease caused by a deficiency of an enzyme called glycogen debranching enzyme, also called alpha-1,6-glucosidase.
The deficiency of debranching enzyme leads to the accumulation of branched glycogen chains (limit dextrins) in the lysosomes of cells of various organs. Symptoms include hepatomegaly and hypoglycemia.
Find Cori Disease and more Glycogen Storage Diseases among Pixorize's visual mnemonics for the USMLE Step 1 and NBME Shelf Exams.