Glycogen Storage Disease Due to Acid Maltase Deficiency, Late-Onset

Alias:

Alpha-1,4-Glucosidase Acid Deficiency, Late-Onset

Gsd Due to Acid Maltase Deficiency, Late-Onset

Glycogen Storage Disease Type Ii, Late-Onset

Glycogen Storage Disease Type 2, Late-Onset

Glycogenosis Type Ii, Late-Onset

Glycogenosis Type 2, Late-Onset

Pompe Disease, Late-Onset

Gsd Type Ii, Late-Onset

Gsd Type 2, Late-Onset

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Glycogen Storage Disease Due to Acid Maltase Deficiency, Late-Onset, is also known as alpha-1,4-glucosidase acid deficiency, late-onset. An important gene associated with Glycogen Storage Disease Due to Acid Maltase Deficiency, Late-Onset is GAA (Alpha Glucosidase). The drugs Miglustat and Glycoside Hydrolase Inhibitors have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle and tongue.

Related ID：

MALACARDS：GLY074