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Osteogenesis imperfecta (OI) is a heterogeneous group of heritable disorders characterized by increased bone fragility. Typical extraskeletal manifestations (hearing loss, blue sclerae, dentinogenesis imperfecta, and hyperlaxity of ligaments and skin) can be variably associated, but no agreed

Cerebral Aneurysms in a Patient with Osteogenesis Imperfecta and Exon 28 Polymorphism of COL1A2