Please use this identifier to cite or link to this item:
https://hdl.handle.net/1/1267
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Forsyth, Cecily J | en |
dc.contributor.other | Favaloro, E.J. | en |
dc.contributor.other | Koutts, J. | en |
dc.date.accessioned | 2019-01-24T03:01:19Z | en |
dc.date.available | 2019-01-24T03:01:19Z | en |
dc.date.issued | 2012-02 | en |
dc.identifier.citation | Volume 34, Issue 1, pp. 102 - 105 | en |
dc.identifier.issn | 1751-5521 | en |
dc.identifier.uri | https://elibrary.cclhd.health.nsw.gov.au/cclhdjspui/handle/1/1267 | en |
dc.description.abstract | Discrimination of types 1 and 2M von Willebrand disease (VWD) is problematic. Type 1 VWD represents a quantitative deficiency of von Willebrand factor and type 2M a qualitative disorder. 2M VWD is considered a potentially more serious bleeding disorder than type 1 VWD and may also require a differential management approach given the higher bleeding risk and that desmopressin may be less effective. We describe a case of 2M VWD 'masquerading' as type 1 and show how the differential diagnosis can be obtained using standard laboratory assays. The case was genetically confirmed as a 3943C>T mutation, leading to R1315C. | en |
dc.subject | Haematology | en |
dc.subject | Hematology | en |
dc.title | Distinguishing types 1 and 2M von Willebrand disease | en |
dc.type | Journal Article | en |
dc.identifier.doi | 10.1111/j.1751-553X.2011.01362.x | en |
dc.description.pubmeduri | https://www.ncbi.nlm.nih.gov/pubmed/21794096 | en |
dc.identifier.journaltitle | International Journal of Laboratory Hematology | en |
dc.relation.orcid | https://orcid.org/0000-0002-9108-3088 | en |
dc.originaltype | Text | en |
item.cerifentitytype | Publications | - |
item.openairetype | Journal Article | - |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.dept | Haematology | - |
Appears in Collections: | Haematology |
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