Orthopaedic and somatic status in patients with osteogenesis imperfecta

Introduction Osteogenesis imperfecta (OI) is a group of rare and relatively diverse genetic disorders, characterized by frequent fractures, bone deformities, low bone mineral density and osteopenia. Frequent fractures, bone deformities, and nonunion are among orthopedic problems in OI patients. Varu...

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Bibliographic Details
Main Authors: Eduard R. Mingazov, Tat'iana V. Ryabykh, Dmitry A. Popkov
Format: Article
Language:English
Published: Russian Ilizarov Scientific Center for Restorative Traumatology and Orthopaedics 2018-06-01
Series:Гений oртопедии
Subjects:
Online Access:http://ilizarov-journal.com/index.php/go/article/view/3395