Massive Coronary Microvascular Dysfunction in Severe Anderson-Fabry Disease Cardiomyopathy

Francesca Graziani, Rosa Lillo, Elena Panaioli, Gionata Spagnoletti, Isabella Bruno, Lucia Leccisotti, Riccardo Marano, Raffaele Manna, Filippo Crea

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

Anderson-Fabry disease (AFD) is a rare genetic lysosomal storage disorder caused by deficient activity of the enzyme α-galactosidase A, leading to progressive intracellular accumulation of neutral glycosphingolipids in different organs, including the heart.
Original languageEnglish
Pages (from-to)N/A-e009104
JournalCIRCULATION. CARDIOVASCULAR IMAGING
Volume12
DOIs
Publication statusPublished - 2019

Keywords

  • Fabry disease
  • galactosidases
  • hypertrophy
  • morbidity
  • mortality

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