Alglucosidase Alfa News

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Alglucosidase Alfa currently has 0 news articles, with 20 predicted indications.

This page combines the AI-predicted indications for Alglucosidase Alfa with the latest health news. Indications highlighted in orange have recent news coverage.

Drug Information

• Original indication: Myozyme is indicated for long-term enzyme-replacement therapy (ERT) in patients with a confirmed diagnosis of Pompe disease (acid-?-glucosidase deficiency). In patients with late-onset Pompe disease...
• Evidence level: L5
• Predicted indications (20):
  • adult polyglucosan body disease (99.5%)
  • glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form (99.3%)
  • glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form (99.3%)
  • congenital entropion (99.2%)
  • congenital ectropion (99.2%)
  • congenital Horner syndrome (disease) (99.2%)
  • ptosis-vocal cord paralysis syndrome (99.2%)
  • camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye (99.1%)
  • epiblepharon (99.1%)
  • ptosis-strabismus-ectopic pupils syndrome (99.1%)
  • tricarboxylic acid cycle disorder (99.1%)
  • ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome (99.0%)
  • mucopolysaccharidosis (99.0%)
  • jaw-winking syndrome (99.0%)
  • disease of transporter activity (99.0%)
  • glycogen storage disease (98.9%)
  • glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form (98.8%)
  • glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form (98.8%)
  • glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form (98.8%)
  • glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form (98.8%)

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Disclaimer: The news on this page is collected automatically and is for research reference only; it does not constitute medical advice.