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Osteogenesis Imperfecta, or “brittle bone disease,” is a genetic condition that affects the body’s ability to produce strong collagen, leading to fragile bones, frequent fractures, skeletal deformities, and chronic pain. In honor of Osteogenesis Imperfecta Awareness Day, we wanted to highlight how this condition impacts not just the skeleton, but everyday life for thousands of people worldwide.#EduTok #TikTokLearningCampaign #LearnOnTikTok
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Tomorrow is #RareDiseaseDay, and we want to raise awareness about some of the rare diseases we work on. Alpha-mannosidosis is a rare lysosomal disorder that can cause frequent infections, developmental delays, muscle weakness, and other symptoms. Age of onset is soon after birth or early in childhood. If you or your loved one is an alpha-mannosidosis patient, connect with ISMRD to gain access to a community of other affected families and stay up to date on the latest research developments. If yo
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TikTokprobably.genetic
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