Cori Disease (Debrancher enzyme deficiency)

What is GSDIII, also called Cori Disease, Forbe’s Disease, or Debrancher Enzyme Deficiency?

Glycogen Storage Disease type 3 is an inherited condition caused by a defect in a gene that controls the breakdown of a complex sugar called glycogen in the body’s cells. Because the glycogen can not be broken down, the accumulated glycogen is structurally abnormal and impairs the function of certain organs and tissues, especially the liver and muscles. It is also called Cori Disease, Forbe’s Disease, or Debrancher Enzyme Deficiency.

For more information on Glycogen Storage Disease Type 3, click here.