Wolff-Parkinson-White and left ventricular noncompaction in a Fabry patient: A case report

Turk Kardiyol Dern Ars. 2016 Apr;44(3):248-50. doi: 10.5543/tkda.2015.92800.

Abstract

Fabry disease is the second most common inherited (X-linked recessive) lysosomal storage disease associated with multiple organ involvement. Cardiac involvement of Fabry disease varies. Successful radiofrequency ablation of a Fabry disease patient with Wolff-Parkinson-White syndrome and left ventricular noncompaction is described in the present report.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Fabry Disease*
  • Female
  • Heart Defects, Congenital*
  • Humans
  • Wolff-Parkinson-White Syndrome*

Supplementary concepts

  • Noncompaction of Left Ventricular Myocardium with Congenital Heart Defects