Legg-Perthes disease in three siblings, two heterozygous and one homozygous for the factor V Leiden mutation
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference16 articles.
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3. Association of antithrombotic factor deficiencies and hypofibrinolysis with Legg-Perthes disease;Glueck;J Bone Joint Surg Am,1996
4. Protein C and S deficiency, thrombophilia, and hypofibrinolysis: pathophysiologic causes of Legg-Perthes disease;Glueck;Pediatr Res,1994
5. Resistance to activated protein C and Legg-Perthes Disease;Glueck;Clin Orthop,1997
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