Difficulties and pitfalls in the laboratory diagnosis of bleeding disorders

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

Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskriftPeer review

Sammanfattning

. 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.
Originalspråkengelska
Sidor (från-till)66-72
TidskriftHaemophilia
Volym18
DOI
StatusPublished - 2012

Ämnesklassifikation (UKÄ)

  • Hematologi

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