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Related Experiment Video

Updated: Jun 3, 2026

In Vivo Quantification of Hip Arthrokinematics during Dynamic Weight-bearing Activities using Dual Fluoroscopy
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Published on: July 2, 2021

Joint hypermobility syndrome: problems that require psychological intervention.

C Baeza-Velasco1, M C Gély-Nargeot, A Bulbena Vilarrasa

  • 1Department of Psychiatry and Legal Medicine, Autonomous University of Barcelona, Barcelona, Spain. c.baezavelasco@gmail.com

Rheumatology International
|March 5, 2011
PubMed
Summary

Joint hypermobility syndrome (JHS), also known as Ehlers-Danlos III, causes significant pain and distress. Psychological interventions are crucial for managing JHS, addressing chronic pain, and improving quality of life.

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Area of Science:

  • Rheumatology
  • Genetics
  • Psychology

Background:

  • Joint hypermobility syndrome (JHS), or Ehlers-Danlos III, is an inherited connective tissue disorder characterized by excessive joint mobility.
  • While considered benign compared to other Ehlers-Danlos types, JHS can be disabling due to pain and distress.

Purpose of the Study:

  • To highlight common challenges in JHS that necessitate psychological intervention.
  • To emphasize the relevance of psychological support in the comprehensive management of JHS.

Main Methods:

  • Literature review and clinical observation.
  • Analysis of psychopathological factors associated with JHS.
  • Exploration of the impact of syndrome recognition on patient well-being.

Main Results:

  • Chronic pain, anxiety, depression, and somatosensory amplification are prevalent in JHS patients.
  • Lack of recognition and knowledge about JHS negatively impacts quality of life.
  • Psychological distress is a significant component of the JHS experience.

Conclusions:

  • JHS management requires addressing psychological aspects alongside physical symptoms.
  • A biopsychosocial approach is essential for effectively treating individuals with JHS.
  • Psychological interventions can alleviate pain, distress, and improve overall quality of life for JHS patients.