Recurrent acute coronary syndrome, polymorphic premature ventricular complexes and a son with a (mis)diagnosis of multiple sclerosis.

Authors

• Nestele, Jeremy¹
• van den Hoven, Carst¹
• Van Craenenbroeck, Emeline M^{1, 2, 3}
• Eyskens, Francois^{4, 5}
• Paelinck, Bernard P^{1, 2}
• Dendooven, Amélie^{6, 7}
• Haine, Steven E^{1, 2, 3}

• ¹ Department of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium. , (Belgium)
• ² Department of Cardiology, Antwerp University Hospital, Edegem, Belgium. , (Belgium)
• ³ Research Group Cardiovascular Diseases, GENCOR, University of Antwerp, Antwerp, Belgium. , (Belgium)
• ⁴ CEMA - Centrum Erfelijke Metabole Aandoeningen, Antwerp University Hospital, Edegem, Belgium. , (Belgium)
• ⁵ CBAA - Centrum Bevolkingsonderzoek voor Aangeboren Aandoeningen Antwerpen, Antwerp University Hospital, Edegem, Belgium. , (Belgium)
• ⁶ Department of Pathology, Antwerp University Hospital, Edegem, Belgium. , (Belgium)
• ⁷ CORE-Center of Oncological REsearch, University of Antwerp, Antwerp, Belgium. , (Belgium)

Type

Published Article

Journal

Acta cardiologica

Publication Date

Sep 01, 2020

Volume

75

Issue

5

Pages

467–468

Identifiers

DOI: 10.1080/00015385.2019.1616137

PMID: 31095450

Source

Medline

Keywords

• Fabry Disease
• Cardiac Phenotype
• Left Ventricular Hypertrophy
• Lysosomal Storage Disorder

Language

English

License

Unknown