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Camurati‐Engelmann disease (CED) is a rare autosomal‐dominant skeletal dysplasia caused by mutations in the transforming growth factor‐β1 (TGFB1) gene. In this study, a retrospective review of patients with CED evaluated at Peking Union Medical College Hospital in Beijing, China, between November 30, 2000 and November 30, 2020 was conducted. Data including demographic data, manifestations, and examination...
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