von Willebrand disease: laboratory aspects of diagnosis and treatment

Haemophilia. 2004 Oct:10 Suppl 4:164-8. doi: 10.1111/j.1365-2516.2004.00979.x.

Abstract

von Willebrand disease is the most common inherited bleeding disorder in humans. VWD can be classified into three major types, designated Types 1, 2 and 3; Type 2 can be further separated into subtypes 2A, 2B, 2M and 2N. The diagnosis of VWD requires a personal and family history of bleeding and confirmation by laboratory analysis. Although Types 2 and 3 are relatively straightforward to diagnose, there may be a risk of overdiagnosis of Type 1 because of an overlap within the normal range. We also report on the clinical profile and diagnosis of VWD in a South American cohort of patients and on the in vitro characteristics of some factor concentrates available for treatment of VWD.

Publication types

  • Review

MeSH terms

  • Adolescent
  • Adult
  • Blood Platelets / chemistry
  • Cohort Studies
  • Factor VIII / analysis
  • Factor VIII / therapeutic use
  • Family Health
  • Female
  • Humans
  • Male
  • Middle Aged
  • Pregnancy
  • Pregnancy Complications, Hematologic / blood
  • Risk Factors
  • von Willebrand Diseases / diagnosis*
  • von Willebrand Diseases / drug therapy
  • von Willebrand Diseases / genetics
  • von Willebrand Factor / analysis

Substances

  • von Willebrand Factor
  • Factor VIII