[Consensus for the study and treatment of Fabry disease. GETER Foundation]

Med Clin (Barc). 2011 Jul 9;137(4):178-83. doi: 10.1016/j.medcli.2011.02.024. Epub 2011 May 6.
[Article in Spanish]
No abstract available

Publication types

  • Practice Guideline

MeSH terms

  • Adolescent
  • Adult
  • Cardiovascular Agents / therapeutic use
  • Child
  • Contraindications
  • Delayed Diagnosis
  • Diagnosis, Differential
  • Disease Management
  • Enzyme Replacement Therapy
  • Fabry Disease / diagnosis
  • Fabry Disease / drug therapy
  • Fabry Disease / epidemiology
  • Fabry Disease / genetics
  • Fabry Disease / therapy*
  • Female
  • Heart Diseases / diagnosis
  • Heart Diseases / drug therapy
  • Heart Diseases / etiology
  • Humans
  • Incidence
  • Infant, Newborn
  • Kidney Failure, Chronic / diagnosis
  • Kidney Failure, Chronic / etiology
  • Kidney Failure, Chronic / therapy
  • Leukocytes / enzymology
  • Lysosomes / enzymology
  • Male
  • Neuralgia / drug therapy
  • Neuralgia / etiology
  • Renal Replacement Therapy
  • alpha-Galactosidase / blood
  • alpha-Galactosidase / genetics
  • alpha-Galactosidase / therapeutic use

Substances

  • Cardiovascular Agents
  • alpha-Galactosidase