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

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, whic...

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Veröffentlicht in:	Journal of bone and joint surgery. American volume 2016-03, Vol.98 (5), p.386-395
Hauptverfasser:	Langereis, Eveline J., den Os, Matthijs M., Breen, Catherine, Jones, Simon A., Knaven, Olga C., Mercer, Jean, Miller, Weston P., Kelly, Paula M., Kennedy, Jim, Ketterl, Tyler G., O’Meara, Anne, Orchard, Paul J., Lund, Troy C., van Rijn, Rick R., Sakkers, Ralph J., White, Klane K., Wijburg, Frits A.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Child Child, Preschool Disease Progression Female Follow-Up Studies Hematopoietic Stem Cell Transplantation Hip Dislocation - diagnostic imaging Hip Dislocation - etiology Hip Dislocation - physiopathology Humans Male Models, Statistical Mucopolysaccharidosis I - complications Mucopolysaccharidosis I - therapy Observer Variation Prognosis Radiography Reproducibility of Results Retrospective Studies Single-Blind Method Treatment Outcome Young Adult
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