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Joint hypermobility syndrome: problems that require psychological intervention

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Abstract

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.

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Authors and Affiliations

  1. Department of Psychiatry and Legal Medicine, Autonomous University of Barcelona, Barcelona, Spain

    C. Baeza-Velasco & A. Bulbena Vilarrasa

  2. Laboratory Epsylon, University Paul Valéry Montpellier 3, Montpellier, France

    M. C. Gély-Nargeot

  3. Faculty of Medicine, University of Chile, Santiago, Chile

    J. F. Bravo

Authors
  1. C. Baeza-Velasco
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  2. M. C. Gély-Nargeot
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  3. A. Bulbena Vilarrasa
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  4. J. F. Bravo
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Correspondence to C. Baeza-Velasco.

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Baeza-Velasco, C., Gély-Nargeot, M.C., Bulbena Vilarrasa, A. et al. Joint hypermobility syndrome: problems that require psychological intervention. Rheumatol Int 31, 1131–1136 (2011). https://doi.org/10.1007/s00296-011-1839-5

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  • DOI: https://doi.org/10.1007/s00296-011-1839-5

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