Heterozygous type I plasminogen deficiency is associated with an increased risk for thrombosis: a statistical analysis in 20 kindreds
The prevalence of thrombosis in patients with heterozygous type I plasminogen deficiency was studied. Fifteen kindreds described in the literature and a further five additional kindreds from the authorsʼ Department were gathered. The prevalence of thrombotic events in all the patients with plasminog...
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Veröffentlicht in: | Blood coagulation & fibrinolysis 1994-12, Vol.5 (6), p.889-893 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The prevalence of thrombosis in patients with heterozygous type I plasminogen deficiency was studied. Fifteen kindreds described in the literature and a further five additional kindreds from the authorsʼ Department were gathered. The prevalence of thrombotic events in all the patients with plasminogen deficiency was 23.6% (22 out of 93 patients), which decreased to 9.5% (seven of 74 patients) when the propositi were excluded. The 95 unaffected siblings were asymptomatic. The comparison between the prevalence of thrombosis in patients with plasminogen deficiency, with or without inclusion of the index patients, and in unaffected family members was statistically significant in both instances (P |
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ISSN: | 0957-5235 1473-5733 |
DOI: | 10.1097/00001721-199412000-00004 |