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pro vyhledávání: '"Carolyn Cook, MD"'
Publikováno v:
Journal of the Pediatric Orthopaedic Society of North America, Vol 9, Iss , Pp 100128- (2024)
Background: Osteogenesis imperfecta (OI), a rare genetic disorder of collagen synthesis and metabolism, is characterized by cortical bone thinning and decreased trabecular bone. We have noted individuals with OI develop radiolucent lesions in the cor
Externí odkaz:
https://doaj.org/article/e6e1e686226144e48b33c6a60bc82186
