Joint hypermobility with and without musculoskeletal complaints: a physiotherapeutic approach (original) (raw)
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Joint hypermobility syndrome: problems that require psychological intervention
Rheumatology International, 2011
Joint Hypermobility Syndrome (JHS), also known as Ehlers-Danlos III, is an inherited disorder of connective tissue, characterised by an exceptional increase in the joint's mobility and the presence of musculoskeletal and other symptoms. It is a benign syndrome if compared with the other types of Ehlers-Danlos, but it can become disabling particularly because it is a significant source of pain and distress. The purpose of this work is to describe some common problems in JHS that render psychological intervention in their overall management relevant. Chronic pain, associated psychopathological factors such as anxiety, depression and somatosensory amplification, and problems arising from a lack of recognition and knowledge of the syndrome, are frequent among those affected, having a negative impact on their quality of life. We emphasise the relevance of addressing JHS from a biopsychosocial approach.
Physiotherapy management of joint hypermobility syndrome—patient and therapist perspectives
Physiotherapy, 2015
Please cite this article as: Palmer S, Terry R, Rimes KA, Clark C, Simmonds J, Horwood J, Physiotherapy management of joint hypermobility syndromendasha focus group study of patient and health professional perspectives, Physiotherapy (2015), http://dx.ABSTRACT 29 Objective: To develop an understanding of patient and health professional views 30 and experiences of physiotherapy to manage joint hypermobility syndrome (JHS).
2012
Introduction: Performing artistes have entertained audiences for thousands of years. Their repertoires require the integration of a well ‘tuned’ central nervous system and hypermobility. Hypermobility is a common phenomenon that is beneficial for some but not for others. This thesis discusses hypermobility associated with multisystemic symptoms referred to as Joint Hypermobility Syndrome (JHS). It is suggested that the multifactorial manifestations of the condition contribute to deconditioning thus impacting on the physical and mental well being of individuals with JHS. Purpose: To explore the multi-factorial manifestations of JHS including functional difficulties and their impact on quality of life. Methods: A two part study; part one, development of a questionnaire to assess for functional difficulties; part two, a mixed methods approach to explore aspects of JHS. Results: Principal Axis Factoring was employed to explore the structure of the 9-item Functional Difficulties Question...