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Fabry disease

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Revision as of 00:39, 11 August 2018 by Penarc (talk | contribs) (1-deoxygalactonojirimycin)
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Fabry disease is a genetic condition involving lysosomal storage (E75.2)[1]

migalastat or 1-deoxygalactonojirimycin received an orphan drug approval [2]

  1. ↑ https://de.wikipedia.org/wiki/Morbus_Fabry
  2. ↑ https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/UCM616598.htm
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