2004
DOI: 10.1007/s10016-003-0087-x
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Deep Venous Thrombosis Caused by Congenital Absence of Inferior Vena Cava, Combined with Hyperhomocysteinemia

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Cited by 61 publications
(90 citation statements)
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“…1 6 Factor V Leiden, prothrombin 20210 and methylenetetrahydrofolate reductase (MTHFR) gene mutation, low protein S levels, high homocysteine concentration and antiphospholipid antibodies represent the thrombophilia subtypes commonly associated with DVT. [4][5][6][7] As illustrated in our case, the patient had an elevated factor VIII level with heterozygous mutation of prothrombin gene and positive lupus anticoagulant.…”
Section: Discussionsupporting
confidence: 56%
“…1 6 Factor V Leiden, prothrombin 20210 and methylenetetrahydrofolate reductase (MTHFR) gene mutation, low protein S levels, high homocysteine concentration and antiphospholipid antibodies represent the thrombophilia subtypes commonly associated with DVT. [4][5][6][7] As illustrated in our case, the patient had an elevated factor VIII level with heterozygous mutation of prothrombin gene and positive lupus anticoagulant.…”
Section: Discussionsupporting
confidence: 56%
“…(3) Absence of the entire IVC, as in our patient's case, suggests that all three paired vein systems failed to develop properly [10], but it has no relation to the other congenital anomalies described previously [11].…”
mentioning
confidence: 65%
“…The hepatic segment drains directly into the right atrium, and the blood from the infrarenal IVC returns to the heart through the azygos and hemiazygos veins [8,10]. There is association with other cardiac and visceral anomalies, such as dextrocardia, atrial septal defect, atrioventricular canal, situsinversus, polysplenia,or asplenia [9,11,12]. …”
Section: Discussionmentioning
confidence: 99%
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