Pompe Disease - Virginia Department of Health
A baby with low acid alpha glucosidase (GAA) activity on their newborn screening specimen(s) may have Glycogen storage disorder type II (Pompe disease). 
Pompe disease - Labcorp Women's HealthChildren with classic infantile-onset Pompe disease will usually have a severe deficiency of the acid alpha-glucosidase enzyme [1]. Without treatment, these ... Pompe Disease: What You Need to Know©2010Pompe Disease. CAUSE. Pompe disease is an inherited condition that affects many different parts of the body. It is a lysosomal storage disorder. When a ... Glycogen Storage Disorder Type II (Pompe)CRIM negative (CN) means there is no residual. GAA enzyme activity. Pompe patients who are. CN produce anti-rhGAA antibodies and do not respond to ERT unless ... Pompe DiseasePompe is also called acid maltase deficiency or glycogen storage disorder type II. It is caused by variants (or mutations) in the GAA gene. This gene carries. Pompe Disease - Wadsworth CenterIt is a lysosomal storage disorder. People with. Pompe disease have problems breaking down a sugar called glycogen. When, glycogen is not broken down, it builds ... Genetic Testing Options for Pompe DiseasePompe disease is a rare but treatable condition that mainly affects the baby's muscles. Individuals with. Pompe disease cannot break down a certain type of. POMPE DISEASE - (Pom-PAY) What is Newborn Screening? - DHHSPompe disease is a recessive genetic condition, and therefore there is not usually a family history of it. My baby was found to have a pseudodeficiency allele. Pompe DiseasePompe Disease is a rare genetic disorder. People with Pompe Disease have a change in a single gene called GAA. Normally, this gene makes the GAA enzyme, which ... Newborn Screening for Pompe Disease - HRSAPompe disease, also known as Glycogen Storage. Disease Type II, is a genetic disorder caused by deficiency of the enzyme acid alpha-glucosidase. (GAA). As a ... Pompe Disease - Illinois Department of Public HealthDefinition. Pompe disease is an inherited metabolic disorder in which harmful amounts of glycogen accumulate within lysosomes of cells. Pompe disease - MedlinePlusPompe disease is an inherited disorder caused by the buildup of a complex sugar called glycogen in the body's cells. Pompe disease - Muscular Dystrophy AssociationPompe is classified as a metabolic muscle disorder, one of a group of diseases that interferes with processing and storage of complex sugars (carbohydrates) ...
