Literature DB >> 20046298

The diagnosis and treatment of von Willebrand disease in children.

Robert J Klaassen1, Jacqueline M Halton.   

Abstract

von Willebrand disease is the most common bleeding disorder seen in children and it affects approximately 1% of the population. Because the bleeding symptoms in von Willebrand disease are generally mild, the diagnosis is often delayed. Prompt diagnosis and management can help to avoid potentially life-threatening bleeding events and unnecessary exposure to blood products. In this review, the various types of von Willebrand disease are outlined, the difficulties in diagnosis are discussed and the therapeutic approach to this common disorder is described.

Entities:  

Keywords:  Child; Factor VIII; von Willebrand disease; von Willebrand factor

Year:  2002        PMID: 20046298      PMCID: PMC2794822          DOI: 10.1093/pch/7.4.245

Source DB:  PubMed          Journal:  Paediatr Child Health        ISSN: 1205-7088            Impact factor:   2.253


  19 in total

1.  Frequency of inherited bleeding disorders in women with menorrhagia.

Authors:  R A Kadir; D L Economides; C A Sabin; D Owens; C A Lee
Journal:  Lancet       Date:  1998-02-14       Impact factor: 79.321

2.  Laboratory assays for von Willebrand factor: relative contribution to the diagnosis of von Willebrand's disease.

Authors:  E J Favaloro; J Koutts
Journal:  Pathology       Date:  1997-11       Impact factor: 5.306

Review 3.  von Willebrand disease in children and adolescents.

Authors:  E J Werner
Journal:  Pediatr Clin North Am       Date:  1996-06       Impact factor: 3.278

4.  Prevalence of von Willebrand disease in children: a multiethnic study.

Authors:  E J Werner; E H Broxson; E L Tucker; D S Giroux; J Shults; T C Abshire
Journal:  J Pediatr       Date:  1993-12       Impact factor: 4.406

Review 5.  Von Willebrand disease in childhood.

Authors:  R Schneppenheim; K B Thomas; A H Sutor
Journal:  Semin Thromb Hemost       Date:  1995       Impact factor: 4.180

Review 6.  Therapy of von Willebrand disease.

Authors:  J P Scott; R R Montgomery
Journal:  Semin Thromb Hemost       Date:  1993       Impact factor: 4.180

7.  DDAVP and epinephrine-induced changes in the localization of von Willebrand factor antigen in endothelial cells of human oral mucosa.

Authors:  M Takeuchi; H Nagura; T Kaneda
Journal:  Blood       Date:  1988-09       Impact factor: 22.113

Review 8.  Molecular mechanism and classification of von Willebrand disease.

Authors:  J E Sadler; T Matsushita; Z Dong; E A Tuley; L A Westfield
Journal:  Thromb Haemost       Date:  1995-07       Impact factor: 5.249

9.  Epidemiological investigation of the prevalence of von Willebrand's disease.

Authors:  F Rodeghiero; G Castaman; E Dini
Journal:  Blood       Date:  1987-02       Impact factor: 22.113

10.  Patterns of development of tachyphylaxis in patients with haemophilia and von Willebrand disease after repeated doses of desmopressin (DDAVP).

Authors:  P M Mannucci; D Bettega; M Cattaneo
Journal:  Br J Haematol       Date:  1992-09       Impact factor: 6.998

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  1 in total

1.  Reevaluation of von Willebrand disease diagnosis in a Croatian paediatric cohort combining bleeding scores, phenotypic laboratory assays and next generation sequencing: a pilot study.

Authors:  Ivana Lapić; Margareta Radić Antolic; Sara Dejanović Bekić; Désirée Coen-Herak; Ernest Bilić; Dunja Rogić; Renata Zadro
Journal:  Biochem Med (Zagreb)       Date:  2022-02-15       Impact factor: 2.313

  1 in total

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