Skeletal features of primary hyperoxaluria type 1, revisited

@article{Hage2008SkeletalFO,
  title={Skeletal features of primary hyperoxaluria type 1, revisited},
  author={Samer El Hage and Ismat Ghanem and Andr{\'e} Baradhi and Chebel Mourani and Samir Mallat and Fernand Dagher and Khalil E. Kharrat},
  journal={Journal of Children's Orthopaedics},
  year={2008},
  volume={2},
  pages={205-210}
}
PurposeThe purpose of this study was to describe the skeletal manifestations of primary hyperoxaluria type 1 (PH1), the most common of the primary hyperoxalurias.MethodsWe clinically and radiographically reviewed 12 consecutive patients diagnosed with PH1, aged between 2 and 17 years. All patients had evidence of some type of renal involvement, 4 of whom were at end-stage renal disease (ESRD) and were under dialysis.ResultsThe main symptom was skeletal pain and was present only in the 4… CONTINUE READING

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Bone impairment in primary hyperoxaluria: a review

Justine Bacchetta, Georges Boivin, Pierre Cochat
  • Pediatric Nephrology
  • 2015
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