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Biological findings in Von Willebrand's pedigrees: implications for inheritance
Thirty-one subjects from three families affected by Von Willebrand's disease have been investigated with the following tests: Ivy's bleeding time; platelet adhesiveness according to Salzman; two-stage factor VIII assay. Twelve patients have a complete form of the disease, i.e., a prolonged...
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Published in: | Journal of clinical pathology 1967-03, Vol.20 (2), p.190-194 |
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creator | Meyer, Dominique Larrieu, Marie-José Maroteaux, Pierre Caen, Jacques P. |
description | Thirty-one subjects from three families affected by Von Willebrand's disease have been investigated with the following tests: Ivy's bleeding time; platelet adhesiveness according to Salzman; two-stage factor VIII assay. Twelve patients have a complete form of the disease, i.e., a prolonged bleeding time with low platelet adhesiveness, and a reduced factor VIII level. Eight subjects have an isolated low platelet adhesiveness associated in three cases with a prolonged bleeding time. The low platelet adhesiveness in these subjects was corrected, as in Von Willebrand's disease, by infusion of haemophilia A plasma. The dominant autosomal mode of inheritance appears to be due to a pleiotropic gene, expressed in a variety of ways |
doi_str_mv | 10.1136/jcp.20.2.190 |
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Twelve patients have a complete form of the disease, i.e., a prolonged bleeding time with low platelet adhesiveness, and a reduced factor VIII level. Eight subjects have an isolated low platelet adhesiveness associated in three cases with a prolonged bleeding time. The low platelet adhesiveness in these subjects was corrected, as in Von Willebrand's disease, by infusion of haemophilia A plasma. The dominant autosomal mode of inheritance appears to be due to a pleiotropic gene, expressed in a variety of ways</description><identifier>ISSN: 0021-9746</identifier><identifier>EISSN: 1472-4146</identifier><identifier>DOI: 10.1136/jcp.20.2.190</identifier><identifier>PMID: 5303273</identifier><identifier>CODEN: JCPAAK</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher><subject>Blood Coagulation Tests ; Blood Platelets ; Factor VIII - analysis ; Genes, Dominant ; Humans ; von Willebrand Diseases - blood ; von Willebrand Diseases - genetics</subject><ispartof>Journal of clinical pathology, 1967-03, Vol.20 (2), p.190-194</ispartof><rights>Copyright BMJ Publishing Group LTD Mar 1967</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b476t-96658ba8ed73e3e50f032250f1ced62e3fe86c000d84f9b3bb806d9d1d08a49c3</citedby><cites>FETCH-LOGICAL-b476t-96658ba8ed73e3e50f032250f1ced62e3fe86c000d84f9b3bb806d9d1d08a49c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC473453/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC473453/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/5303273$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Meyer, Dominique</creatorcontrib><creatorcontrib>Larrieu, Marie-José</creatorcontrib><creatorcontrib>Maroteaux, Pierre</creatorcontrib><creatorcontrib>Caen, Jacques P.</creatorcontrib><title>Biological findings in Von Willebrand's pedigrees: implications for inheritance</title><title>Journal of clinical pathology</title><addtitle>J Clin Pathol</addtitle><description>Thirty-one subjects from three families affected by Von Willebrand's disease have been investigated with the following tests: Ivy's bleeding time; platelet adhesiveness according to Salzman; two-stage factor VIII assay. Twelve patients have a complete form of the disease, i.e., a prolonged bleeding time with low platelet adhesiveness, and a reduced factor VIII level. Eight subjects have an isolated low platelet adhesiveness associated in three cases with a prolonged bleeding time. The low platelet adhesiveness in these subjects was corrected, as in Von Willebrand's disease, by infusion of haemophilia A plasma. The dominant autosomal mode of inheritance appears to be due to a pleiotropic gene, expressed in a variety of ways</description><subject>Blood Coagulation Tests</subject><subject>Blood Platelets</subject><subject>Factor VIII - analysis</subject><subject>Genes, Dominant</subject><subject>Humans</subject><subject>von Willebrand Diseases - blood</subject><subject>von Willebrand Diseases - genetics</subject><issn>0021-9746</issn><issn>1472-4146</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1967</creationdate><recordtype>article</recordtype><recordid>eNp9kcFrFDEUxoNY6lq9eRUGBHtx1mSSSTKCB7votnSxBbWCl5CZvNlmm0mmyazof29kl0U9eHqH7_e99z0-hJ4RPCeE8tebbpxXeF7NSYMfoBlhoioZYfwhmmFckbIRjD9Cj1PaYEyoIPQYHdcU00rQGbo6s8GFte20K3rrjfXrVFhf3ARffLXOQRu1N6epGMHYdQRIbwo7jC4bJht8KvoQM38L0U7ad_AEHfXaJXi6nyfoy4f3nxfn5epqebF4typbJvhUNpzXstUSjKBAocZ9zlPlQTowvALag-QdxthI1jctbVuJuWkMMVhq1nT0BL3d7R237QCmAz9F7dQY7aDjTxW0VX8r3t6qdfiumKCsptn_cu-P4X4LaVKDTR04pz2EbVIyx2wolxl88Q-4Cdvo82-KCIGpZJSwTL3aUV0MKUXoD0kIVr9bUrklVWFVqdxSxp__mf4A72vJernTbZrgx0HW8U5xQUWtPt4s1HJ1KZfXn76p68yf7vh22Pz_8i9JUKqB</recordid><startdate>19670301</startdate><enddate>19670301</enddate><creator>Meyer, Dominique</creator><creator>Larrieu, Marie-José</creator><creator>Maroteaux, Pierre</creator><creator>Caen, Jacques P.</creator><general>BMJ Publishing Group Ltd and Association of Clinical Pathologists</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19670301</creationdate><title>Biological findings in Von Willebrand's pedigrees: implications for inheritance</title><author>Meyer, Dominique ; 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platelet adhesiveness according to Salzman; two-stage factor VIII assay. Twelve patients have a complete form of the disease, i.e., a prolonged bleeding time with low platelet adhesiveness, and a reduced factor VIII level. Eight subjects have an isolated low platelet adhesiveness associated in three cases with a prolonged bleeding time. The low platelet adhesiveness in these subjects was corrected, as in Von Willebrand's disease, by infusion of haemophilia A plasma. The dominant autosomal mode of inheritance appears to be due to a pleiotropic gene, expressed in a variety of ways</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd and Association of Clinical Pathologists</pub><pmid>5303273</pmid><doi>10.1136/jcp.20.2.190</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Blood Coagulation Tests Blood Platelets Factor VIII - analysis Genes, Dominant Humans von Willebrand Diseases - blood von Willebrand Diseases - genetics |
title | Biological findings in Von Willebrand's pedigrees: implications for inheritance |
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