Glycogen Storage Disease Type I

Glycogen storage disease type I, also called von Gierke disease, is an inherited metabolic disorder in which the body cannot properly release glucose stored as glycogen, especially in the liver.

How it presents: It is usually detected in childhood and may be associated with episodes of low blood sugar, enlargement of the liver, and growth difficulties.

Points to consider: Careful management of nutrition, under professional supervision, plays a central role in keeping the body's energy supply stable.

Which specialist treats it? The pediatric gastroenterologist, together with metabolism specialists, follows up on this condition; when signs such as weakness from low blood sugar or a bloated abdomen appear in a child, seeking professional evaluation is the right step.