Abstract
Osteogenesis imperfecta is a widespread hereditary dysplasia of connective tissue, characterized by changes in the bone structure, frequent fractures, manifestations of disorders in other organs and systems. This is a genetically determined disease, characterized by a violation of the production of collagen type 1, for which a specific treatment algorithm has not yet been developed.The article presents scientific data on modern methods of surgical treatment of osteogenesis imperfecta in children using non-telescopic and telescopic intramedullary pins (Rusch nail, titanium elastic rods (TEN), etc.). The article also describes the shortcomings and expected complications after surgical treatment using these metal structures.Key words: incomplete osteogenesis, children, surgical treatment, osteosynthesis, osteotomy, rods.
Sign-in/Register to access full text options 
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
