2017
DOI: 10.1080/14767058.2017.1285892
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Incidences, risk factors and outcomes of neonatal thromboembolism

Abstract: The most common TE was AIS. PC deficiency was the most prevalent inherited risk factor, especially in neonates without precipitating factors.

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Cited by 33 publications
(23 citation statements)
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“…In this study, 63.3% (19/30) of the children presented with obvious cases of the disease, which is far lower than the 85% reported in international studies (10). These results suggest it is necessary to determine other causes, including anti-prothrombin deficiency and protein C or protein S deficiencies (11). The role of polycrystalline, coagulation, and fibrinolysis system gene polymorphisms in the pathogenesis of CVST is currently receiving increased attention.…”
Section: Discussionmentioning
confidence: 99%
“…In this study, 63.3% (19/30) of the children presented with obvious cases of the disease, which is far lower than the 85% reported in international studies (10). These results suggest it is necessary to determine other causes, including anti-prothrombin deficiency and protein C or protein S deficiencies (11). The role of polycrystalline, coagulation, and fibrinolysis system gene polymorphisms in the pathogenesis of CVST is currently receiving increased attention.…”
Section: Discussionmentioning
confidence: 99%
“…PC deficiency is the most common thrombophilia as the cause of pediatric thrombosis in Japan [28]. These patients have one allele or double allele mutations of PROC , and develop hemorrhagic infarction and/or purpura fulminans within two weeks after birth [14, 18], although thrombotic trend depends on the absolute PC activity levels [15]. Because of the varied hemostatic maturation [29], it is difficult to assess the balanced development of coagulation, anticoagulation and fibrinolysis factors during the early postnatal life.…”
Section: Discussionmentioning
confidence: 99%
“…The allele frequency of FVL or FII variant shapes the landscape of molecular epidemiology for inherited thrombosis in Caucasians [911]. By contrast, the absence of FVL or FII variant in East Asia raises the clinical impact of PC, PS, and AT deficiency on thromboembolism in Asian patients [1214]. Severe PC deficiency is a rare thrombophilia.…”
Section: Introductionmentioning
confidence: 99%
“…The annual incidence of CVST in the pediatric population is approximately seven cases per million and is higher in neonates than in children . The sex ratio seems balanced because of the absence of sex‐specific risk factors .…”
Section: Epidemiologymentioning
confidence: 99%