Fabry disease previously diagnosed as Henoch-Schonlein purpura

Korean J Intern Med. 2015 Nov;30(6):925-7. doi: 10.3904/kjim.2015.30.6.925. Epub 2015 Oct 30.
No abstract available

Keywords: Alpha-galactosidase; Fabry disease; Purpura, Schoenlein-Henoch.

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biopsy
  • DNA Mutational Analysis
  • Diagnostic Errors*
  • Enzyme Replacement Therapy
  • Fabry Disease / complications
  • Fabry Disease / diagnosis*
  • Fabry Disease / enzymology
  • Fabry Disease / genetics
  • Genetic Predisposition to Disease
  • Glomerulonephritis, IGA / diagnosis
  • Glomerulonephritis, IGA / etiology
  • Humans
  • IgA Vasculitis / diagnosis*
  • Male
  • Middle Aged
  • Mutation
  • Phenotype
  • Predictive Value of Tests
  • alpha-Galactosidase / genetics
  • alpha-Galactosidase / therapeutic use

Substances

  • GLA protein, human
  • alpha-Galactosidase