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Pompe Disease: Symptoms Treatment - Cleveland Clinic Pompe disease is a genetic condition in which a complex sugar called glycogen builds up in the lysosomes of your body’s cells The disease occurs when you lack a specific digestive enzyme called acid alpha-glucosidase (GAA)
Pompe Disease - Symptoms, Causes, Treatment | NORD Pompe disease is a rare disease continuum with variable rates of disease progression and different ages of onset First symptoms can occur at any age from birth to late adulthood Earlier onset compared to later onset is usually associated with faster progression and greater disease severity
Glycogen storage disease type II - Wikipedia Glycogen storage disease type II (GSD-II), also called Pompe disease, and formerly known as GSD-IIa or Limb–girdle muscular dystrophy 2V, is an autosomal recessive metabolic disorder [1] which damages muscle and nerve cells throughout the body
Pompe Disease | Newborn Screening Find information about newborn screening for Pompe disease, including causes, signs, symptoms, and treatment
Newborn Screening FACT Sheet Pompe Disease The muscle weakness in this disorder leads to serious breathing problems and most children with non-classic infantile-onset Pompe Disease live only into early childhood
Pompe Disease: Symtoms, Causes, Treatments - WebMD Pompe disease happens when your body can't make a protein that breaks down a complex sugar, called glycogen, for energy Too much sugar builds up and damages your muscles and organs Pompe