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Olav Egeberg - arvelig antitrombinmangel og trombofili
Engelsk titel: Olav Egeberg - hereditary antithrombin deficiency and thrombophilia Läs online Författare: Abildgaard U Språk: Nor Antal referenser: 10 Dokumenttyp: Artikel UI-nummer: 01039620 Personnamn som ämnesord: Egeberg O

Tidskrift

Tidsskrift for Den Norske Laegeforening 2001;121(5)604-5 ISSN 0029-2001 E-ISSN 0807-7096 KIBs bestånd av denna tidskrift Denna tidskrift är expertgranskad (Peer-Reviewed)

Sammanfattning

X : In 1965 Olav Egeberg (1916-77) presented the first report that linked a defined, hereditary defect in the control of blood coagulation to thrombotic disease. Having examined a family in which several members had sustained venous thrombosis, he demonstrated that antithrombin activity was clearly subnormal in the affected members. Heparin cofactor activity was also subnormal in these persons. This supported the hypothesis that the two activities might reside in a single protein. The condition was inherited as an autosomal dominant trait. Egeberg's publication initiated thrombophilia as a rewarding research area, and also as an important clinical discipline.