Thromb Haemost 1993; 69(02): 177-184
DOI: 10.1055/s-0038-1651576
Original Article
Von Willebrand Disease
Schattauer GmbH Stuttgart

Von Willebrand Disease: A Database of Point Mutations, Insertions, and Deletions

For the Consortium on von Willebrand Factor Mutations and Polymorphisms[1], and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
David Ginsburg
*   The Howard Hughes Medical Institute, Departments of Internal Medicine and Human Genetics, University of Michigan Medical School, Ann Arbor, MI, USA
,
Evan J Sadler
**   The Howard Hughes Medical Institute, The Jewish Hospital of St. Louis, Departments of Medicine and of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO, USA
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Weitere Informationen

Publikationsverlauf

Received 27. April 1992

Accepted after revision 07. Oktober 1992

Publikationsdatum:
03. Juli 2018 (online)

Summary

The current system for the diagnosis and classification of von Willebrand disease (vWD) is quite complex, with more than 20 distinct variants described. Over the past few years considerable progress has been made toward an understanding of vWD at the molecular level. A small cluster of mutations within the vWF A1 homologous repeat appears responsible for over 90% of type IIB vWD. A similar cluster of mutations in the vWF A2 homologous repeat accounts for the majority of type II A vWD. By RFLP analysis, several type II vWD mutations have been shown to be recurrent on distinct haplotype backgrounds, suggesting independent genetic origins (see accompanying manuscript for a complete list of known polymorphisms). Several mutations at the N-terminus of the mature vWF subunit have been identified in association with abnormal factor VIII binding. Homozygotes for this abnormal vWF present with a hemophilia-like phenotype that is autosomal recessive in inheritance. In a small subset of patients with type III vWD large gene deletions have been identified on one or both vWF alleles. Carriers heterozygous for a deleted locus and one normal vWF gene are generally asymptomatic. Nonsense mutations and other defects resulting in loss of vWF mRNA expression from one allele have also been associated with a recessive type III vWD phenotype. No distinct molecular defect responsible for classic type I vWD has yet been defined.

1 Members of Consortium on von Willebrand Factor Mutations and Polymorphisms. Asterisks denote Steering Committee Members:

1 Takeshi Abe, Tokyo University, Japan; Maria Anvret, Karolinska Hospital, Sweden; Javier Batlle, Hospital Teresa Herrera, Spain; Francesco Bernardi, Universita di Ferrara, Italy; David Bonthron, MRC Human Genetics Unit, Scotland; Derrick Bowen, University of Wales, Wales; Jeroen C. J. Eikenboom, University Hospital Leiden, The Netherlands; Bruce Ewenstein, Brigham and Women’s Hospital, USA; Gunnar Falk, Karolinksa Hospital, Sweden; David Ginsburg,* University of Michigan, USA; Harvey Grainick, National Institutes of Health, USA; Hiroshi Inaba,* Tokyo Medical College, Japan; Aida Inbal,* Beilinson Medical Center, Israel; David Lillicrap,* Queen’s University, Canada; David Mancuso, The Blood Center of Southeastern Wisconsin, USA; Claudine Mazurier,* Laboratoire de Recherche sur l’Hémostase, France; Dominique Meyer,* Hôpital de Bicêtre, France; Jan Michiels, Erasmus University, Rotterdam, The Netherlands; Robert Montgomery,* The Blood Center of Southeastern Wisconsin, USA; Ian Peake,* University of Sheffield, England; Anna M. Randi,* A. Bianchi Bonomi Hemophilia and Thrombosis Center, Italy; J. Evan Sadler,* Washington University, USA; Hidehiko Saito,* Nagoya University, Japan; R. Schneppenheim, Universitäts-Kinderklinik Kiel, Germany; Jan J. Sixma,* Rijksuniversiteit te Utrecht, The Netherlands; Safia Wasi, The Canadian Red Cross, Canada: Gilbert White, University of North Carolina, USA; Paul Winter, Royal Victoria Hospital, Northern Ireland.


 
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