A rare manifestation of Fabry's disease

Swiss Med Wkly. 2007 Feb 24;137(7-8):130. doi: 10.4414/smw.2007.11649.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Amino Acid Substitution / genetics
  • Fabry Disease / genetics
  • Fabry Disease / pathology*
  • Humans
  • Male
  • Paresis / genetics
  • Paresis / pathology*
  • Stroke / genetics
  • Stroke / pathology*
  • alpha-Galactosidase / genetics

Substances

  • alpha-Galactosidase