Document Detail


A review of long-term prophylaxis in the rare inherited coagulation factor deficiencies.
MedLine Citation:
PMID:  19906159     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The rare inherited coagulation factor deficiencies (deficiencies of factors I, II, V, VII, XI, XIII, combined FV + FVII deficiency, combined deficiency of the vitamin K dependent factors and von Willebrand disease type 3) have an aggregate prevalence of approximately 1:100,000. They may cause recurrent life or function threatening haemorrhage. In this article we review the available literature on long-term prophylaxis and, where possible, make recommendations on this important area.
Authors:
T Todd; D J Perry
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Publication Detail:
Type:  Journal Article; Review     Date:  2009-11-11
Journal Detail:
Title:  Haemophilia : the official journal of the World Federation of Hemophilia     Volume:  16     ISSN:  1365-2516     ISO Abbreviation:  Haemophilia     Publication Date:  2010 Jul 
Date Detail:
Created Date:  2010-07-20     Completed Date:  2011-01-05     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9442916     Medline TA:  Haemophilia     Country:  England    
Other Details:
Languages:  eng     Pagination:  569-83     Citation Subset:  IM    
Affiliation:
Department of Haematology, Royal Devon and Exeter Hospital, Exeter, UK. anthony.todd@rdeft.nhs.uk
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MeSH Terms
Descriptor/Qualifier:
Blood Coagulation Disorders / drug therapy*
Blood Coagulation Factors / administration & dosage,  therapeutic use*
Fibrinogen
Humans
Vitamin K Deficiency / drug therapy
Chemical
Reg. No./Substance:
0/Blood Coagulation Factors; 9001-32-5/Fibrinogen

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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