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http://dx.doi.org/10.2106/00004623-199406000-00016 | DOI Listing |
J Orthop Case Rep
September 2020
Department of Orthopaedics, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
Introduction: Melorheostosis, on its own, is an extremely uncommon disease. It is non-hereditary, sclerosing bone lesion affecting the adjacent soft tissues. Long bones are commonly involved.
View Article and Find Full Text PDFSkeletal Radiol
January 2017
School of Medicine, Pathology Department, Gaziosmanpasa University, Tokat, Turkey.
Dysplasia epiphysealis hemimelica (DEH) is a rare developmental disorder characterized by osteocartilaginous overgrowth in one or more epiphyses. The disease usually involves a single limb or is hemimelic (lateral or medial compartment), and lower extremities are more frequently affected than upper extremities. Here we present clinical and radiological findings for a male DEH patient at 1.
View Article and Find Full Text PDFRev Chir Orthop Reparatrice Appar Mot
October 2002
Service de Rhumatologie B, Hôpital El Ayachi, CHU Avicenne, Rabat-Salé, Maroc, France.
Fibrous dysplasia is an uncommon condition characterized by the presence of mesenchymatous tissue in bone. There are various risks. We describe the clinical and radiological features observed in a patient with fibrous polyostotic fibrous dysplasia and discuss risks.
View Article and Find Full Text PDFEur J Pediatr Surg
June 1998
Department of Orthopedic Pediatric Surgery, Hôpital de l'Archet, Nice, France.
Melorheostosis is a rare bone dysplasia, exceptionally described in childhood. It has been discovered in a 12-year-old boy who had a hemimelic affection associated with straw-berry skin marks. A 25 mm inequality of length of the lower limbs and a valgus deformation of the ankle resulting in a claudication and gonalgia requiring surgical correction.
View Article and Find Full Text PDFJ Bone Joint Surg Am
June 1994
Shriners Hospital for Crippled Children, Portland Unit, Oregon 97201.
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