Langerhans’ cell histiocytosis (LCH) is manifested in a variety of ways, the most common
being the eosinophilic granuloma, a localized, often solitary bone lesion that occurs …

Objective This study was undertaken to describe the imaging characteristics of synovial
hemangioma, with the goal of improving the disappointing rate (22%) of clinical diagnosis of this …

Thirteen cases of osteoid osteoma and nine cases of osteoblastoma are reported. Diagnostic
difficulties of osteoblastoma are illustrated by the versatile radiographic appearances of …

Osteogenesis imperfecta (OI) is a heritable disease of bone with low bone mass and bone
fragility. The disease is generally classified into four types based on clinical features and …

Dysplasia epiphysealis hemimelica (DEH) is an osteocartilaginous overgrowth involving one
or multiple epiphyses or ossification centers, usually in a lower extremity on one side of the …

Infection of the pediatric musculoskeletal system still constitutes a diagnostic and therapeutic
challenge. Antibiotic therapy has a high success rate in most bacterial infections. Key …

This multicenter collaborative study was undertaken to review the types and complications
of femoral neck fractures in children. It is a retrospective clinical and radiological review of …

OBJECTIVES: To determine the prevalence of and the risk factors for vertebral fractures in a
cohort of children with chronic rheumatic diseases considered at risk for osteopenia. STUDY …

We present a 3‐generation family, ascertained after the birth of a child with cleidocranial
dysplasia (CCD). The propositus presented with respiratory distress (due to a narrow thorax) …

Keutel syndrome is a rare autosomal recessive disorder characterized by diffuse cartilage
calcification, characteristic physiognomy, brachytelephalangism, peripheral pulmonary …