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Article

Recurrent ischemic cerebrovascular events in a patient with type I antithrombin deficiency caused by 9788 G>A splice site mutation: a case report.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Mar 2013

Szymańska Magdalena, Alhenc-Gelas Martine, Undas Anetta

Abstract excerpt

Type I antithrombin deficiency is an autosomal dominant disorder associated with high risk for venous thromboembolism. Data on the association between antithrombin deficiency and arterial thromboembolism are inconsistent. We report here the case of AT deficiency in a 43-year-old man free of cardiovascular risk factors who experienced venous thromboembolism and ischemic stroke followed by two transient ischemic...

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PMID: 23358206
DOI: 10.1097/MBC.0b013e32835b2467

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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