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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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Bibliografiske detaljer
Udgivet i:BMC Musculoskelet Disord
Main Authors: Arponen, Heidi, Mäkitie, Outi, Waltimo-Sirén, Janna
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2014
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4300610/
https://ncbi.nlm.nih.gov/pubmed/25494634
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2474-15-428
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