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Ollier disease, also known as multiple enchondromatosis, is a rare genetic disorder characterized by multiple benign cartilage-forming tumors (enchondromas) in the bones. The literature review discusses the general features of Ollier disease including its pathogenesis, clinical presentations, diagnosis through radiological findings and histopathology, and treatment options which include surgical excision and filling the cavity to prevent fractures. While Ollier disease is typically non-hereditary, its irreg

Author

Cass

Language

EN