Thromb Haemost 1983; 50(04): 864-868
DOI: 10.1055/s-0038-1665330
Original Article
Schattauer GmbH Stuttgart

Differences Between Heterozygous Dominant and Recessive von Willebrand’s Disease Type I Expressed by Bleeding Symptoms and Combinations of Factor VIII Variables

T B Wahlberg
The Dept of Blood Coagulation Disorders, Karolinska Hospital, Stockholm, Sweden
,
M Blombäck
The Dept of Blood Coagulation Disorders, Karolinska Hospital, Stockholm, Sweden
,
Z M Ruggeri
1   The Depts of Immunology and of Basic and Clinical Research, Scripps Clinic and Research Foundation, La Jolla, California, U.S.A.
› Author Affiliations
Further Information

Publication History

Received 21 January 1983

Accepted 10 October 1983

Publication Date:
18 July 2018 (online)

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Summary

Three families with von Willebrand’s disease (vWd) type I were investigated. A reliable identification of healthy and diseased individuals was achieved by number of bleeding symptoms, assays of bleeding time, FVIII:C (one stage and two stage), VIIIR: Ag (EIA) and ristocetin cofactor. The diagnoses - vWd or non-vWd were confirmed by laboratory indices based on predictive values of positive and negative tests, also including VIIIR: Ag (IRMA and RIA). The last mentioned two variables did not contribute to significantly better identification of vWd versus health. The best single test variable for this purpose was ristocetin cofactor. One vWd family had significantly higher levels of ristocetin cofactor and shorter bleeding time than the other two vWd families and is probably the typical example of a family transmitting classical severe vWd.