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Difficulties and pitfalls in the laboratory diagnosis of bleeding disorders

In English

Författare

  • P. H. B. Bolton-Maggs
  • E. J. Favaloro
  • Andreas Hillarp
  • I. Jennings
  • H. P. Kohler

Summary, in English

. von Willebrand disease (VWD) is the most common inherited bleeding disorder, but variable severity and several classification types mean that diagnosis is often not straightforward. In many countries, the assays are not readily available and/or are not well standardized. The latest methods and the basis of VWD are discussed here, together with information from the international quality assessment programme (IEQAS). Factor XIII deficiency is a rare, but important bleeding disorder, which may be missed or diagnosed late. A discussion and update on this diagnosis is considered in the final section of our review.

Publiceringsår

2012

Språk

Engelska

Sidor

66-72

Publikation/Tidskrift/Serie

Haemophilia

Volym

18

Dokumenttyp

Artikel i tidskrift

Förlag

Wiley-Blackwell

Ämne

  • Hematology

Nyckelord

  • bleeding disorders
  • external quality assurance
  • factor XIII deficiency
  • laboratory diagnosis
  • von Willebrand disease

Status

Published

Forskningsgrupp

  • Clinical Chemistry, Malmö

ISBN/ISSN/Övrigt

  • ISSN: 1351-8216