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Oorerflike faktor V gebrek (Parahemofilie) : 'n gevalbespreking

dc.contributor.authorBrink S.
dc.date.accessioned2011-03-18T14:59:58Z
dc.date.available2011-03-18T14:59:58Z
dc.date.issued1974
dc.identifier.citationBrink, S. 1974. Oorerflike Faktor V Gebrek (Parahemofilie) : 'n gevalbespreking. South African Medical Journal, 16 March: 537-539.
dc.identifier.issn0256-9574 (print) 2078-5135 (online)
dc.identifier.urihttp://hdl.handle.net/10019.1/8170
dc.descriptionArticle
dc.descriptionThe original publication is available at http://www.samj.org.za
dc.description.abstractA white boy and his family were investigated for a haemorrhagic diathesis. Both he and his sister, a primipara between 26 and 28 wk pregnant, in May 1973 had a total lack of factor V, demonstrated an abnormal partial thromboplastin time and a prolonged prothrombin index with normal prothrombin activity. Factor V assays were 10%. Clotting screening tests on the father and another son, who are both heterozygote carriers, were within normal limits, but the specific factor V assays were 48 and 39% respectively, which demonstrates the limitations of routine screening tests as opposed to specific factor V assays. The hereditary patterns in the two documented families in South Africa, and this family, are consistent with a partial dominancy.
dc.format.extentp. 537-539 : ill.
dc.language.isoaf_ZAaf_ZA
dc.publisherHMPG
dc.subjectBlood clotting factor 5
dc.subjectBleeding disorder -- Genetic aspects
dc.subjectBlood clotting factor 5 deficiency
dc.subjectHaemophilia -- Genetic aspects
dc.subjectHeterozygote
dc.titleOorerflike faktor V gebrek (Parahemofilie) : 'n gevalbesprekingaf_ZA
dc.title.alternativeInherited factor V deficiency (Parahaemophilia): a case reporten_ZA
dc.typeArticle
dc.description.versionPublishers' version
dc.rights.holderThe author


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