2004
DOI: 10.1097/00043426-200407000-00003
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Symptomatic Thrombosis in Turkish Neonates

Abstract: The pathogenesis of thrombosis in neonates is multi-factorial. Along with underlying diseases or triggering events, congenital prothrombotic factors (FV G1691A and PT G20210A) showed a trend toward a higher frequency in neonates with thrombosis. These data indicate that mutations associated with underlying disorders in neonates may contribute to the development of thromboembolic disease.

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Cited by 8 publications
(8 citation statements)
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“…Male sex is proposed as a risk factor, with more embolization occurring in males than females [6,7,10,[12][13][14]28,29,[46][47][48][49][50][51], but this is inconsistent across studies [35]. Of the 83 reported cases, 19 newborns were female (23%), 24 were male (29%), and in 40 (48%) the sex was unspecified.…”
Section: Congenital Risk Factorsmentioning
confidence: 99%
“…Male sex is proposed as a risk factor, with more embolization occurring in males than females [6,7,10,[12][13][14]28,29,[46][47][48][49][50][51], but this is inconsistent across studies [35]. Of the 83 reported cases, 19 newborns were female (23%), 24 were male (29%), and in 40 (48%) the sex was unspecified.…”
Section: Congenital Risk Factorsmentioning
confidence: 99%
“…Various risk factors for thrombosis in newborns have been reported in the literature. In a study by Gurgey and colleagues [32], which consisted of 26 newborns with thrombosis, patients with an infection were largest group, and those with hypoxia were the second-largest group. Another study by Nowak-Gottl and colleagues [31], which consisted of 79 newborns with thrombosis, showed that the largest patient groups had a central venous catheter, spontaneous thrombosis, and infection, respectively.…”
Section: Incidence Of Thrombosismentioning
confidence: 99%
“…The congenital prothrombotic disorders that have been linked to TEs in newborns include deficiencies of antithrombin, protein C, protein S and plasminogen and the presence of prothrombin gene 20210A and Factor V Leiden. 3 The methylene tetrahydrofolate reductase (MTHFR) C677T genotype found in our patient has been positively associated with arterial and venous thrombotic disease in some populations; however, this mutation alone may not sufficiently explain this arterial clot. 4,5 The use of HBOT has been shown by several investigators to restore a favorable cellular environment for wound healing and support vascular proliferation by increasing the oxygen content of the plasma.…”
Section: Case Presentationmentioning
confidence: 73%