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High prevalence of inherited prothrombotic risk factors in 134 consecutive patients with von Willebrand disease
We screened 134 consecutive patients with von Willebrand disease (VWD) (106 type 1, 26 type 2, and 2 type 3 VWD) for the most important inherited prothrombotic risk factors. One hundred eight patients (80.6%) weree positive for at least one of the prothrombotic risk factors screened for. A high prev...
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Published in: | American journal of hematology 2006-06, Vol.81 (6), p.465-467 |
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creator | Franchini, Massimo Veneri, Dino Poli, Giovanni Manzato, Franco Salvagno, Gian Luca Lippi, Giuseppe |
description | We screened 134 consecutive patients with von Willebrand disease (VWD) (106 type 1, 26 type 2, and 2 type 3 VWD) for the most important inherited prothrombotic risk factors. One hundred eight patients (80.6%) weree positive for at least one of the prothrombotic risk factors screened for. A high prevalence of prothrombin G20210A (10.5%) and factor V Leiden (11.9%) mutations was found with allele frequencies of 5.2 and 6%, respectively. Three carriers of multiple prothrombotic gene mutations experienced a thrombotic event. Our study suggests that the recent evidence of an association between inherited thrombotic and hemorrhagic disorders also holds true in VWD patients. Am. J. Hematol. 81:465–467, 2006. © 2006 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/ajh.20623 |
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One hundred eight patients (80.6%) weree positive for at least one of the prothrombotic risk factors screened for. A high prevalence of prothrombin G20210A (10.5%) and factor V Leiden (11.9%) mutations was found with allele frequencies of 5.2 and 6%, respectively. Three carriers of multiple prothrombotic gene mutations experienced a thrombotic event. Our study suggests that the recent evidence of an association between inherited thrombotic and hemorrhagic disorders also holds true in VWD patients. Am. J. 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One hundred eight patients (80.6%) weree positive for at least one of the prothrombotic risk factors screened for. A high prevalence of prothrombin G20210A (10.5%) and factor V Leiden (11.9%) mutations was found with allele frequencies of 5.2 and 6%, respectively. Three carriers of multiple prothrombotic gene mutations experienced a thrombotic event. Our study suggests that the recent evidence of an association between inherited thrombotic and hemorrhagic disorders also holds true in VWD patients. Am. J. Hematol. 81:465–467, 2006. © 2006 Wiley‐Liss, Inc.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>bleeding</subject><subject>Factor V - genetics</subject><subject>Female</subject><subject>Gene Frequency - genetics</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hemorrhage - genetics</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Platelet diseases and coagulopathies</subject><subject>Point Mutation</subject><subject>Prevalence</subject><subject>Prothrombin - genetics</subject><subject>Risk Factors</subject><subject>thrombosis</subject><subject>Thrombosis - genetics</subject><subject>von Willebrand disease</subject><subject>von Willebrand Diseases - genetics</subject><issn>0361-8609</issn><issn>1096-8652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LAzEQhoMoWqsH_4DkouChmo82mxylqFUEL4rHJclO3Oh2U5O00n9vtAVPnmYYHt7hfRA6oeSSEsKu9Ht7yYhgfAcNKFFiJMWE7aIB4YKWnagDdJjSOyGUjiXZRwdUCEkqrgYozPxbixcRVrqD3gIODvu-hegzNOUechvD3ITsLY4-fWCnbQ4xFQhTPsY29AnsMvsV4IXOHvqc8JfPLV6FHr_6rgMTdd_gxifQCY7QntNdguPtHKKX25vn6Wz0-HR3P71-HFkuJR9pB-AmzDXgGtkwPqYWGOMV5YYyYZWpGu6YMKKixChFGLeqotIYMtZSKsmH6HyTWyp8LiHleu6Tha7TPYRlqkt_rirJC3ixAW0MKUVw9SL6uY7rmpL6x25d7Na_dgt7ug1dmjk0f-RWZwHOtoBOVneuNLc-_XFVpZSa_ARdbbgv38H6_4_19cNs8_obCcGR1w</recordid><startdate>200606</startdate><enddate>200606</enddate><creator>Franchini, Massimo</creator><creator>Veneri, Dino</creator><creator>Poli, Giovanni</creator><creator>Manzato, Franco</creator><creator>Salvagno, Gian Luca</creator><creator>Lippi, Giuseppe</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200606</creationdate><title>High prevalence of inherited prothrombotic risk factors in 134 consecutive patients with von Willebrand disease</title><author>Franchini, Massimo ; Veneri, Dino ; Poli, Giovanni ; Manzato, Franco ; Salvagno, Gian Luca ; Lippi, Giuseppe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3883-afeef52fdefd8d2341ce223713b126c9b7d3f26b6710b99023c9718bb04a88983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>bleeding</topic><topic>Factor V - genetics</topic><topic>Female</topic><topic>Gene Frequency - genetics</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hemorrhage - genetics</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Platelet diseases and coagulopathies</topic><topic>Point Mutation</topic><topic>Prevalence</topic><topic>Prothrombin - genetics</topic><topic>Risk Factors</topic><topic>thrombosis</topic><topic>Thrombosis - genetics</topic><topic>von Willebrand disease</topic><topic>von Willebrand Diseases - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Franchini, Massimo</creatorcontrib><creatorcontrib>Veneri, Dino</creatorcontrib><creatorcontrib>Poli, Giovanni</creatorcontrib><creatorcontrib>Manzato, Franco</creatorcontrib><creatorcontrib>Salvagno, Gian Luca</creatorcontrib><creatorcontrib>Lippi, Giuseppe</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Franchini, Massimo</au><au>Veneri, Dino</au><au>Poli, Giovanni</au><au>Manzato, Franco</au><au>Salvagno, Gian Luca</au><au>Lippi, Giuseppe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High prevalence of inherited prothrombotic risk factors in 134 consecutive patients with von Willebrand disease</atitle><jtitle>American journal of hematology</jtitle><addtitle>Am J Hematol</addtitle><date>2006-06</date><risdate>2006</risdate><volume>81</volume><issue>6</issue><spage>465</spage><epage>467</epage><pages>465-467</pages><issn>0361-8609</issn><eissn>1096-8652</eissn><coden>AJHEDD</coden><abstract>We screened 134 consecutive patients with von Willebrand disease (VWD) (106 type 1, 26 type 2, and 2 type 3 VWD) for the most important inherited prothrombotic risk factors. One hundred eight patients (80.6%) weree positive for at least one of the prothrombotic risk factors screened for. A high prevalence of prothrombin G20210A (10.5%) and factor V Leiden (11.9%) mutations was found with allele frequencies of 5.2 and 6%, respectively. Three carriers of multiple prothrombotic gene mutations experienced a thrombotic event. Our study suggests that the recent evidence of an association between inherited thrombotic and hemorrhagic disorders also holds true in VWD patients. Am. J. Hematol. 81:465–467, 2006. © 2006 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>16680739</pmid><doi>10.1002/ajh.20623</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Biological and medical sciences bleeding Factor V - genetics Female Gene Frequency - genetics Hematologic and hematopoietic diseases Hemorrhage - genetics Humans Male Medical sciences Platelet diseases and coagulopathies Point Mutation Prevalence Prothrombin - genetics Risk Factors thrombosis Thrombosis - genetics von Willebrand disease von Willebrand Diseases - genetics |
title | High prevalence of inherited prothrombotic risk factors in 134 consecutive patients with von Willebrand disease |
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