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Fabry Disease

  • First described in 1898 by Johannes Fabry, German dermatologist
  • Lysosomal storage disorder
  • Second most common lysosomal storage disorder
  • α-galactosidase A deficient activity
  • Accumulation of glycosphingolipids (vascular endothelium, smooth-muscles, ganglia)
  • >300 mutations
  • X-linked (men harboring the major disease manifestations)