What is another word for Pompe Disease?
Pronunciation: [pˈɒmp dɪzˈiːz] (IPA) 
Pompe disease, also known as glycogen storage disease type II, is a rare genetic disorder caused by a deficiency in the enzyme acid alpha-glucosidase (GAA). This results in the buildup of glycogen in the body's cells, especially in the muscles. Pompe disease can lead to progressive muscle weakness, respiratory problems, and even death, especially if left untreated.
There are few synonyms for Pompe disease as it is a relatively uncommon disorder. However, it is sometimes referred to as acid maltase deficiency, due to the lack of the GAA enzyme. Additionally, some sources may refer to the disease as glycogenosis type II or glycogen storage disease type II. Despite the lack of synonyms, it is important for medical professionals and patients alike to be familiar with Pompe disease and its potential symptoms in order to establish a proper diagnosis and receive appropriate treatment.
