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• W3127766488 abstract "Pompe disease is an autosomal recessive lysosomal glycogen storage disorder caused by the deficiency of acid alpha-glucosidase and subsequent progressive glycogen accumulation due to mutations in the GAA gene. Pompe disease manifests with a broad spectrum of disease severity, ranging from severe infantile-onset diseases such as hypotonia and hypertrophic cardiomyopathy to late-onset diseases such as myopathy and respiratory compromise. The diagnosis requires demonstration of deficiency of the lysosomal acid alpha-glucosidase enzyme, which can be assayed in dried blood spot or liquid blood samples, together with supportive biomarker tests, and confirmed with molecular genetic analysis. Targeted screening of at-risk populations and universal newborn screening can result in earlier diagnosis and enable earlier treatment initiation, which result in the potential improvement of clinical outcomes. Disease-modifying treatment with enzyme replacement therapy has partially altered the natural history of the disease, but more efficacious novel therapies are under evaluation including second-generation enzyme replacement therapies, molecular chaperones and gene therapy approaches. Long-term survivors with Pompe disease are now manifesting novel aspects of the disease including widespread vascular disease, smooth muscle and central nervous system involvement, and these emerging phenotypes will require additional specific therapeutic approaches." @default.
• W3127766488 created "2021-02-15" @default.
• W3127766488 creator A5032904426 @default.
• W3127766488 date "2020-10-02" @default.
• W3127766488 modified "2023-10-03" @default.
• W3127766488 title "Advances in diagnosis and management of Pompe disease." @default.
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• W3127766488 doi "https://doi.org/10.34763/jmotherandchild.20202402si.2001.000002" @default.
• W3127766488 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8518093" @default.
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