Von Gierke Disease

Von Gierke disease is an inherited metabolic disorder, known as glycogen storage disease type I, in which the body cannot properly release stored glucose, which causes difficulty maintaining stable blood sugar levels.

Common cause: it is due to a genetic alteration that affects an enzyme needed to process glycogen, a substance that serves as an energy reserve.

Common manifestations: episodes of low blood sugar, an increase in the size of the liver, slower growth and abnormalities in some laboratory tests.

Which specialist treats it? its management falls to the endocrinologist together with the pediatrician, who monitor the child's metabolism and development. It is advisable that any suspicion be confirmed and followed by a professional who knows the case thoroughly.