Publication:
Double trouble: myocardial infarction with non-obstructive coronary arteries as a presentation of Hughes syndrome in monozygotic twins

dc.contributor.authorDjokovic, A. (42661226500)
dc.contributor.authorStojanovich, L. (55917563000)
dc.contributor.authorStanisavljevic, N. (36163559700)
dc.contributor.authorPopovic, M. (57197354363)
dc.contributor.authorZdravkovic, M. (24924016800)
dc.date.accessioned2025-06-12T14:28:00Z
dc.date.available2025-06-12T14:28:00Z
dc.date.issued2020
dc.description.abstractMyocardial infarction with non-obstructive coronary arteries (MINOCA) is a recently described, clinically significant entity, with prevalence rates ranging from 1% to 14% and a mean of 6% of all patients with myocardial infarction. Antiphospholipid syndrome (APS; Hughes syndrome) is characterized by the presence of antiphospholipid antibodies associated with thrombosis (arterial and/or venous) and/or pregnancy morbidity and could be the cause of MINOCA. Data on genetic predisposition to APS are scarce. The present study describes a unique case of monozygotic twin brothers who, at a young age, developed the same clinical presentation of APS. The diagnosis of APS was later confirmed, along with a diagnosis of systemic lupus erythematosus in one brother. © The Author(s) 2020.
dc.identifier.urihttps://doi.org/10.1177/0961203320906267
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85079531845&doi=10.1177%2f0961203320906267&partnerID=40&md5=dc23a76c50a0956e87427276b302ca68
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/4965
dc.subjectAntiphospholipid syndrome
dc.subjectMINOCA
dc.subjectsystemic lupus erythematosus
dc.titleDouble trouble: myocardial infarction with non-obstructive coronary arteries as a presentation of Hughes syndrome in monozygotic twins
dspace.entity.typePublication

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