Recurrent neuropathy associated with Ehlers–Danlos syndrome

@article{Voermans2005RecurrentNA,
  title={Recurrent neuropathy associated with Ehlers–Danlos syndrome},
  author={Nicol C. Voermans and G. W. Drost and Albert van Kampen and A. A. Gabre{\"e}ls–Festen and Martin Lammens and Ben C J Hamel and Joost Schalkwijk and Baziel G. M. van Engelen},
  journal={Journal of Neurology},
  year={2005},
  volume={253},
  pages={670-671}
}
Sirs: The Ehlers-Danlos syndromes (EDS) are a group of heritable connective tissue disorders characterized by articular hypermobility, skin hyperextensibility and tissue fragility resulting in recurrent joint dislocations, vascular lesions, easy bruising, and excessive scarring [1]. The hypermobility type of EDS is restricted to mild skin involvement and generalized joint hypermobility [2]. EDS is associated with deficiency of extracellular-matrix proteins such as collagen I, III and V and… CONTINUE READING
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