Hip Dysplasia in Children With Osteogenesis Imperfecta: Association With Collagen Type I C-Propeptide Mutations

BACKGROUND: Osteogenesis imperfecta (OI) is a heritable skeletal disorder characterized by bone fragility and short stature that is usually due to mutations in 1 of the 2 genes that code for collagen type I α-chains. The association between hip dysplasia and OI has not been systematically investigat...

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Detalles Bibliográficos
Autores principales: Kishta, Waleed, Abduljabbar, Fahad H., Gdalevitch, Marie, Rauch, Frank, Hamdy, Reggie, Fassier, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2017
Materias:
Lower Extremity
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5592982/
https://www.ncbi.nlm.nih.gov/pubmed/26371943
http://dx.doi.org/10.1097/BPO.0000000000000644

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5592982/
https://www.ncbi.nlm.nih.gov/pubmed/26371943
http://dx.doi.org/10.1097/BPO.0000000000000644

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