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The session was on Osteogenesis Imperfecta, is a heterogeneous a rare connective tissue disorder commonly caused by mutations in the collagen type I genes. Pharmacological treatment has been most extensively studies in children, and there are only few studies comprising adult OI patients.
The NIDAS webinar creates awareness among people especially parents and caregivers of the individuals with disability, and thus provides a platform to share their concerns and clear doubts. For more than two years, NIDAS has been successful in creating awareness regarding various aspects of disability and associated issues.
