ArticleEuropean heart journal. Case reports2019
Spontaneous coronary artery dissection in a patient with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy syndrome: a case report.
Article in European heart journal. Case reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed, 5 citations in OpenAlex.
- Article
- Spontaneous coronary artery dissection with leucoencephalopathy associated with thrombospondin Type 1 domain containing 1 gene mutation: a case report.European heart journal. Case reports · 2023Article
- Management of Coronary Artery Disease in CADASIL Patients: Review of Current Literature.Medicina (Kaunas, Lithuania) · 2023Review
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
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Abstract
backgroundCerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) syndrome is a genetically inherited condition most notably affecting the central nervous system in young adults. There is limited knowledge on its association with coronary arteries, and its association with spontaneous coronary artery dissection (SCAD) has not been previously reported. CASE SUMMARY: A 61-year-old woman who is known to have CADASIL syndrome presented with anterior ST-segment myocardial infarction and underwent emergency angiography. This showed appearance consistent with SCAD in the mid left anterior descending artery with tubular stenosis. DISCUSSION: The association between CADASIL syndrome and SCAD has not been previously reported. The similarity in the underlying pathophysiology of these two conditions makes this case intriguing.
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