CLINICAL CASE OF RARE TYPE V OSTEOGENESIS IMPERFECTA

Osteogenesis imperfecta, also known as the brittle bone disease, is a clinically heterogenic hereditary connective tissue disease characterized by brittle bones and high risk of skeletal bone fractures. Other observable symptoms, such as deformities of limb and spinal bones, blue sclerae, dentinogen...

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Bibliographic Details
Published in:Педиатрическая фармакология
Main Authors: G. T. Yakhyayeva, T. V. Margieva, L. S. Namazova-Baranova, K. V. Savostyanov, A. A. Pushkov, N. V. Zhurkova, K. V. Zherdev, N. D. Vashakmadze, A. K. Gevorkyan
Format: Article
Language:Russian
Published: Union of pediatricians of Russia 2015-08-01
Subjects:
osteogenesis imperfecta
pseudosarcoma
bone fracture
fibrocartilage callus
densitometry
bisphosphonate
bone brittleness
alphacalcidol
ifitm5
bril
children
Online Access:https://www.pedpharma.ru/jour/article/view/472

Internet

https://www.pedpharma.ru/jour/article/view/472

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