Re-writing the natural history of pain and related symptoms in the joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type.

@article{Castori2013RewritingTN,
  title={Re-writing the natural history of pain and related symptoms in the joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type.},
  author={Marco Castori and Silvia Morlino and Claudia Celletti and Giulia Ghibellini and Michela Bruschini and Paola Grammatico and Carlo Blundo and Filippo Camerota},
  journal={American journal of medical genetics. Part A},
  year={2013},
  volume={161A 12},
  pages={2989-3004}
}
Joint hypermobility syndrome (JHS) and Ehlers-Danlos syndrome, hypermobility type (EDS-HT) are two clinically overlapping connective tissue disorders characterized by chronic/recurrent pain, joint instability complications, and minor skin changes. Fatigue and headache are also common, although are not yet considered diagnostic criteria. JHS/EDS-HT is a unexpectedly common condition that remains underdiagnosed by most clinicians and pain specialists. This results in interventions limited to… CONTINUE READING