Difficulties and pitfalls in the laboratory diagnosis of bleeding disorders
(2012) In Haemophilia 18. p.66-72- Abstract
- . 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.
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/2883854
- author
- Bolton-Maggs, P. H. B. ; Favaloro, E. J. ; Hillarp, Andreas LU ; Jennings, I. and Kohler, H. P.
- organization
- publishing date
- 2012
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- bleeding disorders, external quality assurance, factor XIII deficiency, laboratory diagnosis, von Willebrand disease
- in
- Haemophilia
- volume
- 18
- pages
- 66 - 72
- publisher
- John Wiley & Sons Inc.
- external identifiers
-
- wos:000305605400012
- scopus:84862883345
- ISSN
- 1351-8216
- DOI
- 10.1111/j.1365-2516.2012.02830.x
- language
- English
- LU publication?
- yes
- id
- dd407f39-7b3b-4cdb-8889-a4f4702260fb (old id 2883854)
- date added to LUP
- 2016-04-01 10:31:35
- date last changed
- 2025-04-04 14:00:46
@article{dd407f39-7b3b-4cdb-8889-a4f4702260fb, abstract = {{. 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.}}, author = {{Bolton-Maggs, P. H. B. and Favaloro, E. J. and Hillarp, Andreas and Jennings, I. and Kohler, H. P.}}, issn = {{1351-8216}}, keywords = {{bleeding disorders; external quality assurance; factor XIII deficiency; laboratory diagnosis; von Willebrand disease}}, language = {{eng}}, pages = {{66--72}}, publisher = {{John Wiley & Sons Inc.}}, series = {{Haemophilia}}, title = {{Difficulties and pitfalls in the laboratory diagnosis of bleeding disorders}}, url = {{http://dx.doi.org/10.1111/j.1365-2516.2012.02830.x}}, doi = {{10.1111/j.1365-2516.2012.02830.x}}, volume = {{18}}, year = {{2012}}, }