TY - JOUR
T1 - Difficulties and pitfalls in the laboratory diagnosis of bleeding disorders
AU - Bolton-Maggs, P. H. B.
AU - Favaloro, E. J.
AU - Hillarp, Andreas
AU - Jennings, I.
AU - Kohler, H. P.
PY - 2012
Y1 - 2012
N2 - . 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.
AB - . 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.
KW - bleeding disorders
KW - external quality assurance
KW - factor XIII deficiency
KW - laboratory diagnosis
KW - von Willebrand disease
UR - https://www.scopus.com/pages/publications/84862883345
U2 - 10.1111/j.1365-2516.2012.02830.x
DO - 10.1111/j.1365-2516.2012.02830.x
M3 - Article
SN - 1351-8216
VL - 18
SP - 66
EP - 72
JO - Haemophilia
JF - Haemophilia
ER -