Absence of congenital prethrombotic disorders in children with Legg-Perthes disease

Citation
N. Sirvent et al., Absence of congenital prethrombotic disorders in children with Legg-Perthes disease, J PED ORT B, 9(1), 2000, pp. 24-27
Citations number
18
Categorie Soggetti
Ortopedics, Rehabilitation & Sport Medicine
Journal title
JOURNAL OF PEDIATRIC ORTHOPAEDICS-PART B
ISSN journal
1060152X → ACNP
Volume
9
Issue
1
Year of publication
2000
Pages
24 - 27
Database
ISI
SICI code
1060-152X(200001)9:1<24:AOCPDI>2.0.ZU;2-M
Abstract
Resistance to activated protein C (RPCA) and other congenital prethrombotic disorders have been recently reported to be strongly associated with Legg- Perthes disease. RPCA and deficiencies of protein C, protein S, and antithr ombin III were sought in 22 children with Legg-Perthes disease. Detection o f the factor V Leiden mutation was found in children with RPCA. Twenty-two healthy children paired by age and sex served as controls. The prevalence o f congenital prethrombotic disorders was not found to differ significantly among patients with Legg-Perthes disease and among control subjects. Only o ne patient had RPCA; this patient was heterozygous for the factor V Leiden mutation. Twenty patients and all the control subjects had entirely normal coagulation results. The authors conclude that unless more data become avai lable, RPCA and deficiencies of protein C, protein S, and antithrombin III should not be considered associated with Legg-Perthes disease.