Severe hypertrophic cardiomyopathy in a patient with atypical Anderson-Fabry disease

Future Cardiol. 2017 Nov;13(6):521-527. doi: 10.2217/fca-2017-0011. Epub 2017 Sep 22.

Abstract

Aim: Anderson-Fabry disease (AFD) is a hereditary disorder caused by a deficiency in the lysosomal enzyme α-galactosidase A which causes dysfunctions in multiple organ systems. Cardiac manifestation includes left ventricular hypertrophy, thickening of the valves, conduction disturbances and in the late phase, extensive areas of myocardial fibrosis with increased risk of sudden cardiac death. Case example: A case of AFD with exclusive cardiac involvement is described. During follow-up, due to the high risk of life-threatening arrhythmic events, implantation of an implantable cardioverter defibrillator is performed.

Conclusion: AFD patients with advanced cardiac disease might represent a subgroup of patients who may require an implantable cardioverter defibrillator for primary prevention of sudden cardiac death.

Keywords: Anderson-Fabry disease; cardiac magnetic resonance; cardiomyopathies; echocardiography; enzymatic replacement therapy; sudden cardiac death.

Publication types

  • Case Reports

MeSH terms

  • Cardiomyopathy, Hypertrophic / diagnostic imaging*
  • Cardiomyopathy, Hypertrophic / etiology
  • Cardiomyopathy, Hypertrophic / therapy*
  • Death, Sudden, Cardiac / prevention & control*
  • Defibrillators, Implantable
  • Echocardiography / methods
  • Electrocardiography / methods
  • Fabry Disease / complications*
  • Fabry Disease / diagnosis
  • Follow-Up Studies
  • Humans
  • Isoenzymes / therapeutic use
  • Magnetic Resonance Imaging, Cine / methods
  • Male
  • Middle Aged
  • Multimodal Imaging / methods*
  • Rare Diseases
  • Risk Assessment
  • Severity of Illness Index
  • Treatment Outcome
  • alpha-Galactosidase / therapeutic use*

Substances

  • Isoenzymes
  • alpha-Galactosidase