Overview

Imagine living in a body where a simple fall, a bump, or even a sudden sneeze could cause a bone to break. This is the daily reality for those with osteogenesis imperfecta, often called ""Brittle Bone Disease."" This book takes you inside their world, revealing the challenges, resilience, and triumphs of individuals and families navigating life with fragile bones. From the moment a child is diagnosed to the ongoing journey of managing fractures, deformities, and mobility limitations, this book explores the full spectrum of OI. You'll discover the science behind the condition, including the role of collagen, genetic mutations, and the different types of inheritance that shape its severity. Through real-life stories, illustrative examples, and detailed explanations, readers gain an intimate understanding of what it means to live with OI-the daily challenges, the emotional impact, and the coping strategies that empower individuals to lead meaningful lives. Beyond the personal stories, this book dives deep into diagnosis, treatment options, and emerging therapies. Learn about bisphosphonates, surgical interventions, physical therapy, and the groundbreaking potential of gene therapy and stem cell innovations. GRAB YOUR COPY NOW!

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