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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: 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
Sprache:Inglês
Veröffentlicht: Paediatrician Publishers, LLC 2015-08-01
Schriftenreihe:Pediatričeskaâ Farmakologiâ
Schlagworte:
osteogenesis imperfecta
pseudosarcoma
bone fracture
fibrocartilage callus
densitometry
bisphosphonate
bone brittleness
alphacalcidol
ifitm5
bril
children
Online Zugang:https://www.pedpharma.ru/jour/article/view/472
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge