Document Detail


Type 2N von Willebrand disease due to compound heterozygosity for R854Q and a novel R763G mutation at the cleavage site of von Willebrand factor propeptide.
MedLine Citation:
PMID:  16953269     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Type 2N von Willebrand disease (VWD) is characterized by a markedly decreased affinity of von Willebrand factor (VWF) for factorVIII (FVIII) and is caused by mutations in the D' or D3 domain of mature VWF. We now report a French patient with an atypical 2N VWD phenotype associating FVIII deficiency with plasmaVWF unable to bind FVIII (undetectableVWF:FVIIIB) but with an abnormal multimeric profile. This patient is heterozygous for both the frequent R854Q type 2NVWD mutation and a novel R763G mutation at the cleavage site between VWF propeptide and mature VWF. Four children of the patient displayed moderately decreased VWF:FVIIIB of plasma VWF and were heterozygous for either the R763G or the R854Q mutation. Children with the R763G mutation displayed the same abnormal multimeric profile as their father. Recombinant VWF (rVWF) expression studies performed in COS-7 cells showed that the R763G mutation subtly affects its multimeric profile and dramatically impairs its FVIII binding function. Furthermore, the characteristics of hybrid G763/Q854 rVWF resulting from cotransfection experiments were in agreement with the type 2N VWD diagnosis of the patient. We conclude that R763G is a new type 2N VWD mutation located in the VWF propeptide which alters the proteolytic processing of VWF and consequently its binding to FVIII.
Authors:
Lysiane Hilbert; Paquita Nurden; Claudine Caron; Alan T Nurden; Jenny Goudemand; Dominique Meyer; Edith Fressinaud; Claudine Mazurier;
Related Documents :
12754709 - Molecular detection of novel wfs1 mutations in patients with wolfram syndrome by a dhpl...
8044659 - Difference in frequencies of the cystic fibrosis alleles, delta f508 and w1282x, betwee...
17273969 - Mutations in cohesin complex members smc3 and smc1a cause a mild variant of cornelia de...
18608099 - Alsod: the amyotrophic lateral sclerosis online database.
7505689 - Direct sequencing of the complete cftr gene: the molecular characterisation of 99.5% of...
11896459 - Somatic mosaicism for a mecp2 mutation associated with classic rett syndrome in a boy.
9066799 - Dna hybridization evidence for the principal lineages of hummingbirds (aves:trochilidae).
6874139 - Flow karyotype analysis and fluorescence-activated sorting of burkitt-lymphoma-associat...
1570349 - Population genetics of the fragile-x syndrome: multiallelic model for the fmr1 locus.
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Thrombosis and haemostasis     Volume:  96     ISSN:  0340-6245     ISO Abbreviation:  Thromb. Haemost.     Publication Date:  2006 Sep 
Date Detail:
Created Date:  2006-09-05     Completed Date:  2007-01-12     Revised Date:  2009-11-19    
Medline Journal Info:
Nlm Unique ID:  7608063     Medline TA:  Thromb Haemost     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  290-4     Citation Subset:  IM    
Affiliation:
Laboratoire français du Franctionnement et des Biotechnologies, Lille, France. hilbert@lfb.fr
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Aged
Animals
Binding Sites
COS Cells
Cercopithecus aethiops
Factor VIII / chemistry*
Heterozygote*
Humans
Male
Mutation*
Peptides / chemistry*
Recombinant Proteins / chemistry
Sequence Analysis, DNA
von Willebrand Diseases / diagnosis*,  genetics*
von Willebrand Factor / genetics*
Chemical
Reg. No./Substance:
0/Peptides; 0/Recombinant Proteins; 0/von Willebrand Factor; 9001-27-8/Factor VIII

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Preeclampsia and pregnancy loss in women with a history of venous thromboembolism and prophylactic l...
Next Document:  Amino acid regions 572-579 and 657-666 of the spacer domain of ADAMTS13 provide a common antigenic c...