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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Autors principals: 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
Idioma:Inglês
Publicat: Paediatrician Publishers, LLC 2015-08-01
Col·lecció:Pediatričeskaâ Farmakologiâ
Matèries:
osteogenesis imperfecta
pseudosarcoma
bone fracture
fibrocartilage callus
densitometry
bisphosphonate
bone brittleness
alphacalcidol
ifitm5
bril
children
Accés en línia:https://www.pedpharma.ru/jour/article/view/472
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