Log in to save to my catalogue

Spontaneous coronary artery dissection with leucoencephalopathy associated with thrombospondin Type...

Spontaneous coronary artery dissection with leucoencephalopathy associated with thrombospondin Type...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2860616681

Spontaneous coronary artery dissection with leucoencephalopathy associated with thrombospondin Type 1 domain containing 1 gene mutation: a case report

About this item

Full title

Spontaneous coronary artery dissection with leucoencephalopathy associated with thrombospondin Type 1 domain containing 1 gene mutation: a case report

Journal title

European heart journal. Case reports, 2023, Vol.7 (9), p.ytad419-ytad419

Language

English

Formats

More information

Scope and Contents

Contents

BackgroundSpontaneous coronary artery dissection (SCAD) is increasingly diagnosed as one of the infrequent causes of acute coronary syndrome. Almost no cause was identified in half of the cases. Here, we report a rare case of spontaneous coronary artery dissection with leucoencephalopathy (SCADLE) associated with a mutation of the thrombospondin Ty...

Alternative Titles

Full title

Spontaneous coronary artery dissection with leucoencephalopathy associated with thrombospondin Type 1 domain containing 1 gene mutation: a case report

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2860616681

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2860616681

Other Identifiers

E-ISSN

2514-2119

DOI

10.1093/ehjcr/ytad419

How to access this item