The fabry cardiomyopathy: Models for the cardiologist

Academic Article

Abstract

  • Fabry disease is an X-linked lysosomal storage disorder caused by α-galactosidase A deficiency. Intracellular accumulation of globotriaosylceramide starts in utero and progressively develops in various tissues and organs. Cardiac involvement is frequent, and its presentation as concentric nonobstructive left ventricular hypertrophy serves as a model for other hypertrophic cardiomyopathies. This review describes the Fabry cardiomyopathy, its treatment, and multidisciplinary patient care models. These models will help clinicians in diagnosing, assessing, and treating patients with Fabry disease. As the models can be extrapolated to other diseases, they might contribute to more optimal clinical management of patients with other cardiac disorders. © 2011 by Annual Reviews. All rights reserved.
  • Authors

    Published In

    Digital Object Identifier (doi)

    Author List

  • Weidemann F; Niemann M; Warnock DG; Ertl G; Wanner C
  • Start Page

  • 59
  • End Page

  • 67
  • Volume

  • 62