Purpose or Case Report: Osteogenesis imperfecta (OI) is a rare genetic disorder that affects bone development and structure, resulting in bone fragility and susceptibility to fractures. This educational exhibit offers a comprehensive examination of OI, with particular emphasis on the clinical types I, II, III, IV, and V. With a focus on diagnostic tools, management strategies, and emerging treatments, this exhibit aims to enhance the understanding of OI within the pediatric radiology community. We will present a detailed overview of OI types, emphasizing the genetic and clinical variations that distinguish them. Attendees will gain insights into the pathophysiology of OI and its impact on bone health, growth, and overall well-being in affected children. We will highlight imaging techniques and genetic testing that facilitate accurate diagnosis and characterization of OI types. Through case studies, we will demonstrate the pivotal role of radiologists in early detection and improved patient outcomes. Treatment modalities for OI, including bisphosphonates, orthopedic interventions, and emerging therapies, will be explored. Our goal is to empower pediatric radiologists with the knowledge and tools necessary to provide accurate and timely diagnosis as well as to contribute to optimal disease management, ongoing research,
and advancements in the field. By focusing on OI in all its diverse manifestations, this exhibit aims to strengthen the expertise of pediatric radiologists in identifying, characterizing, and managing this complex condition. Our collective effort in enhancing the care of children with OI will ultimately improve their quality of life and future prospects.
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