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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Paediatrician Publishers, LLC 2015-08-01
Cyfres:Pediatričeskaâ Farmakologiâ
Pynciau:
osteogenesis imperfecta
pseudosarcoma
bone fracture
fibrocartilage callus
densitometry
bisphosphonate
bone brittleness
alphacalcidol
ifitm5
bril
children
Mynediad Ar-lein:https://www.pedpharma.ru/jour/article/view/472
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