Thromb Haemost 1980; 43(01): 002-005
DOI: 10.1055/s-0038-1649998
Original Article
Schattauer GmbH Stuttgart

Variant von Willebrand’s Disease

A Study Emphasizing Crossed-Immunoelectrophoresis
David Green
The Atherosclerosis Program, Rehabilitation Institute of Chicago, and the Hematology Section, Department of Medicine, Northwestern University Medical School, U.S.A.
,
K J Philip
The Atherosclerosis Program, Rehabilitation Institute of Chicago, and the Hematology Section, Department of Medicine, Northwestern University Medical School, U.S.A.
› Author Affiliations
Further Information

Publication History

Received 11 June 1979

Publication Date:
13 July 2018 (online)

Summary

30 members of an Illinois kindred were studied with a battery of haemostatic tests including the template bleeding time, platelet retention by glass beads (PRGB), measurement of activities related to factor VIII, and crossed-immunoelectrophoresis (CIEP). 9 family members had a history of excessive bleeding, and all 9 had prolonged bleeding times and increased migration of their factor VIII-related antigen (VIIIR:Ag) on CIEP. Of the other tests performed, the VIII: Ristocetin Cofactor and the PRGB showed the best correlation with the bleeding time. 3 subjects who were not bleeders, but who came from a branch of the family where there were several affected members, also had an abnormal VIIIR: Ag. The pattern of inheritance of the altered VIIIR: Ag in this family was one of autosomal dominance with full penetrance. The CIEP is a valuable screening test for the detection of variant von Willebrand’s disease and the recognition of silent heterozygotes.

 
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