Progression of Hip Dysplasia in Mucopolysaccharidosis Type I Hurler After Successful Hematopoietic Stem Cell Transplantation.

@article{Langereis2016ProgressionOH,
  title={Progression of Hip Dysplasia in Mucopolysaccharidosis Type I Hurler After Successful Hematopoietic Stem Cell Transplantation.},
  author={Eveline J. Langereis and Matthijs M den Os and Catherine Breen and Simon A. Jones and O. C. Knaven and Jean Mercer and W P Miller and Paula Marie Kelly and Jim Kennedy and Tyler G Ketterl and Anne O'meara and Paul J Orchard and Troy C Lund and Rick Robert van Rijn and Ralph J. B. Sakkers and Klane K White and Frits A. Wijburg},
  journal={The Journal of bone and joint surgery. American volume},
  year={2016},
  volume={98 5},
  pages={
          386-95
        }
}
  • Eveline J. Langereis, Matthijs M den Os, +14 authors Frits A. Wijburg
  • Published in
    The Journal of bone and joint…
    2016
  • Medicine
  • BACKGROUND Dysostosis multiplex contributes substantially to morbidity in patients with Hurler syndrome (mucopolysaccharidosis type I Hurler phenotype [MPS I-H]), even after successful hematopoietic stem cell transplantation (HSCT). One of the hallmarks of dysostosis multiplex in MPS I-H is hip dysplasia, which often requires surgical intervention. We sought to describe in detail the course of hip dysplasia in this group of patients, as assessed by radiographic analysis, and to identify… CONTINUE READING

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    References

    Publications referenced by this paper.
    SHOWING 1-10 OF 33 REFERENCES

    Longterm outcome of Hurler syndrome patients after hematopoietic cell transplantation: an international multicenter study

    • AldenhovenM, RF Wynn, +18 authors JJ. Boelens
    • 2015
    VIEW 1 EXCERPT