Microvascular angina as prehypertrophic presentation of fabry disease cardiomyopathy

Circulation

Volumn 130, Issue 17, 2014, Pages 1530-1531

  Frustaci, Andrea ^a,b   Russo, Matteo A ^c   Francone, Marco ^a   Chimenti, Cristina ^a,b  

^a SAPIENZA UNIVERSITY OF ROME   (Italy)

^b NATIONAL INSTITUTE FOR INFECTIOUS DISEASES L SPALLANZANI   (Italy)

^c IRCCS SAN RAFFAELE PISANA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLSALICYLIC ACID; AGALSIDASE ALFA; ALPHA GALACTOSIDASE; DILTIAZEM;

ADULT; ANGIOCARDIOGRAPHY; CARDIOMYOPATHY; CARDIOVASCULAR MAGNETIC RESONANCE; CASE REPORT; ELECTROCARDIOGRAM; ENDOTHELIAL DYSFUNCTION; ENZYME ACTIVITY; ENZYME REPLACEMENT; FABRY DISEASE; FEMALE; GENE MUTATION; HEART CATHETERIZATION; HEART LEFT VENTRICLE HYPERTROPHY; HEART LEFT VENTRICLE WALL; HUMAN; NEW YORK HEART ASSOCIATION CLASS; NOTE; PRECORDIAL PAIN; PRIORITY JOURNAL; SYNDROME X; THORAX PAIN; ANGINA PECTORIS; CARDIAC IMAGING; COMPLICATION; MICROCIRCULATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOLOGY; PATHOPHYSIOLOGY; PHYSIOLOGY;

ADULT; ANGINA PECTORIS; CARDIAC IMAGING TECHNIQUES; FABRY DISEASE; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MICROCIRCULATION;

EID: 84922042485     PISSN: 00097322     EISSN: 15244539     Source Type: Journal    
DOI: 10.1161/CIRCULATIONAHA.114.012178     Document Type: Note

References (2)

1. Desnick RJ, Ioannou YA, Eng CM: Alpha-Galactosidase A deficiency: Fabry disease. The Metabolic and Molecular Bases of Inherited Disease.. Edited by Scriver CR, Beaudet AL, Sly WS, Valle D, Kinzler KE, Vogelstein B. New York, McGraw-Hill, 2001, pp 3733-3774.
2. Chimenti C, Morgante E, Tanzilli G, Mangieri E, Critelli G, Gaudio C, Russo MA, Frustaci A. Angina in Fabry disease reflects coronary small vessel disease. Circ Heart Fail. 2008;1:161-169.