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Bleeding symptoms and laboratory correlation in patients with severe von Willebrand disease
- Source :
- Haemophilia : the official journal of the World Federation of Hemophilia. 15(4)
- Publication Year :
- 2009
-
Abstract
- Type 3 von Willebrand disease (VWD) is a rare bleeding disorder with markedly decreased or absent von Willebrand factor (VWF) protein, accompanied by a parallel decrease in VWF function and factor VIII (FVIII) activity. The goal of this study was to describe the population of patients enrolled in the USA Centers for Disease Control Universal Data Collection (UDC) study with type 3 VWD, defined as a VWF:Ag of
- Subjects :
- Male
congenital, hereditary, and neonatal diseases and abnormalities
medicine.medical_specialty
Adolescent
Genotype
Population
Hemorrhage
Gastroenterology
Severity of Illness Index
Young Adult
Von Willebrand factor
hemic and lymphatic diseases
Internal medicine
Arthropathy
Severity of illness
Hemarthrosis
von Willebrand Factor
medicine
Von Willebrand disease
Humans
Young adult
education
Child
Genetics (clinical)
education.field_of_study
biology
business.industry
Clinical Laboratory Techniques
Hematology
General Medicine
Bleed
medicine.disease
United States
Surgery
von Willebrand Diseases
Child, Preschool
biology.protein
Female
business
Body mass index
Subjects
Details
- ISSN :
- 13652516
- Volume :
- 15
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Haemophilia : the official journal of the World Federation of Hemophilia
- Accession number :
- edsair.doi.dedup.....0d7d6196d97546354e8ca71b85a22080