Clinic Case of Rare Type VI Osteogenesis Imperfecta

Clinic Case of Rare Type VI Osteogenesis Imperfecta

Osteogenesis imperfect is genetically heterogeneous group of diseases which are characterized by bone brittleness and fractures. It was thought for a long time that this is happening due to mutations in collagen genes. However, within past decade the understanding of osteogenesis imperfecta etiology...

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Bibliographic Details
Main Authors: Olga N. Ignatovich, Leyla S. Namazova-Baranova, Tea V. Margieva, Natalia V. Zhurkova, Kirill V. Savostyanov, Alexander V. Pushkov
Format: Article
Language:English
Published: Paediatrician Publishers, LLC 2019-04-01
Series:Pediatričeskaâ Farmakologiâ
Subjects:
osteogenesis imperfecta type vi
serpinf1 gene
pigment epithelium-derived factor (pedf)
children
Online Access:https://www.pedpharma.ru/jour/article/view/1693

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