|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
6
|
|
pubmed:dateCreated |
2010-1-11
|
|
pubmed:abstractText |
von Willebrand disease (VWD) type 3 is a rare disorder characterized by absent or <0.1 UmL(-1) of ristocetin cofactor (VWF:RCo), and a very low level of factor VIII (FVIII:C). A total absence of FVIII:C has never been reported in type 3 VWD. This case illustrates the effect of severe von Willebrand factor (VWF) deficiency on the factor VIII level.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Nov
|
|
pubmed:issn |
1365-2516
|
|
pubmed:author |
|
|
pubmed:issnType |
Electronic
|
|
pubmed:volume |
15
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
1258-61
|
|
pubmed:meshHeading |
pubmed-meshheading:19563498-Circumcision, Male,
pubmed-meshheading:19563498-Diagnostic Errors,
pubmed-meshheading:19563498-Factor VIII,
pubmed-meshheading:19563498-Female,
pubmed-meshheading:19563498-Genes, Recessive,
pubmed-meshheading:19563498-Genotype,
pubmed-meshheading:19563498-Hemophilia A,
pubmed-meshheading:19563498-Hemostatics,
pubmed-meshheading:19563498-Humans,
pubmed-meshheading:19563498-Infant,
pubmed-meshheading:19563498-Male,
pubmed-meshheading:19563498-Pedigree,
pubmed-meshheading:19563498-Postoperative Hemorrhage,
pubmed-meshheading:19563498-von Willebrand Disease, Type 3,
pubmed-meshheading:19563498-von Willebrand Factor
|
|
pubmed:year |
2009
|
|
pubmed:articleTitle |
Undetected factor VIII in a patient with type 3 von Willebrands disease mistaken as severe haemophilia A.
|
|
pubmed:affiliation |
Department of Pediatric Hematology-Oncology, McMaster University, Hamilton, ON, Canada.
|
|
pubmed:publicationType |
Journal Article,
Case Reports
|
