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
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: Artigo
Language:Inglês
Published: Paediatrician Publishers, LLC 2015-08-01
Series:Pediatričeskaâ Farmakologiâ
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
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