Accurate prognosis for pediatric osteogenesis imperfecta remains elusive despite advances

Osteogenesis imperfecta, also known as “brittle bone disease,” is a rare genetic condition frequently diagnosed in childhood and typically caused by mutations in COL1A1 and COL1A2 genes.Historically, Ricki S. Carroll, MD, MBE, skeletal dysplasia and palliative care pediatrician at Nemours Children’s Hospital, Delaware, told Healio the severity of osteogenesis imperfecta (OI) was

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