Osteogenesis Imperfecta: Diagnostic Feature

• Main Authors: Olga N. Ignatovich (Author), Leyla S. Namazova-Baranova (Author), Тea V. Мargieva (Author), Guzal Т. Yakhyaeva (Author), Natalia V. Zhurkova (Author), Кirill V. Savostyanov (Author), Alexander A. Pushkov (Author), Ivan A. Krotov (Author)
• Formato: Livro
• Publicado em: Union of pediatricians of Russia, 2018-07-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: Connect to this object online.

Osteogenesis imperfect (OI) is a rare genetic disease of connective tissue, the main manifestation are fractures that are developing due to increased bone fragility in both children and adults. Currently, it is known that the genetic basis of the disease in 90% of cases are violations in the genes C...