Association between joint hypermobility, scoliosis, and cranial base anomalies in paediatric Osteogenesis imperfecta patients: a retrospective cross-sectional study

BACKGROUND: Joint hypermobility is a common clinical characteristic of patients with Osteogenesis imperfecta (OI), a disorder with serious comorbidities of scoliosis and cranial base anomalies. This study aimed at evaluating how prevalent joint hypermobility is in paediatric OI patients, and to find...

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Detalles Bibliográficos
Autores principales: Arponen, Heidi, Mäkitie, Outi, Waltimo-Sirén, Janna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300610/
https://www.ncbi.nlm.nih.gov/pubmed/25494634
http://dx.doi.org/10.1186/1471-2474-15-428

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300610/
https://www.ncbi.nlm.nih.gov/pubmed/25494634
http://dx.doi.org/10.1186/1471-2474-15-428

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