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PMID: 15357789 Published · ppublish English Journal Article Review

The rare coagulation disorders--review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation.

Haemophilia : the official journal of the World Federation of Hemophilia ·Vol. 10 ·No. 5 ·2004-09-00 ·Pages 593-628

Bolton-Maggs PH, Perry DJ, Chalmers EA, Parapia LA, Wilde JT, Williams MD, Collins PW, Kitchen S, Dolan G, Mumford AD

Abstract

The rare coagulation disorders are heritable abnormalities of haemostasis that may present significant difficulties in diagnosis and management. This review summarizes the current literature for disorders of fibrinogen, and deficiencies of prothrombin, factor V, FV + VIII, FVII, FX, the combined vitamin K-dependent factors, FXI and FXIII. Based on both collective clinical experience and the literature, guidelines for management of bleeding complications are suggested with specific advice for surgery, spontaneous bleeding, management of pregnancy and the neonate. We have chosen to include a section on Ehlers-Danlos Syndrome because haematologists may be consulted about bleeding manifestations in such patients.

MeSH Terms
Afibrinogenemia/diagnosis,genetics,therapy Blood Coagulation Disorders/diagnosis,therapy Clinical Laboratory Techniques Coagulation Protein Disorders/diagnosis,therapy Hemorrhagic Disorders/etiology,therapy Humans Hypoprothrombinemias/diagnosis,therapy Practice Guidelines as Topic Vitamin K Deficiency/diagnosis,therapy
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Bolton-Maggs P H B
Department of Clinical Haematology, Manchester Royal Infirmary, Manchester, UK. paula.bolton-maggs@man.ac.uk
Perry D J
Chalmers E A
Parapia L A
Wilde J T
Williams M D
Collins P W
Kitchen S
Dolan G
Mumford A D
Article Info
Journal
Haemophilia : the official journal of the World Federation of Hemophilia
Abbr.
Haemophilia
ISSN
1351-8216
Published
2004-09-00
Pages
593-628
Language
English
Region
England
NLM ID
9442916
Subset
IM
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