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CaseReport Article

Enthesopathy as the presenting feature of X-linked hypophosphatemia: A case report

Pages 221-223 | Received 19 Jul 1992, Accepted 08 Oct 1992, Published online: 08 Jul 2009

References

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  • Burnstein M. I., Lawson J. P., Kottamasu S. R., Ellis B. I., Micho J. The enthesopathic changes of hypophosphatemic oste‐omalacia in adults: radiologic findings. AJR Am J Roentgenol 1989; 153(4)785–90
  • Hardy D. C., Murphy W. A., Siegel B. A., Reid I. R., Whyte M. P. X‐linked hypophosphatemia in adults: prevalence of skeletal, radiographic and scintigraphic features. Radiology 1989; 171(2)403–14
  • Polisson R. P., Martinez S., Khoury M., Harrell R. M., Lyles K. W., Friedman N., Harrelson J. M., Reisner E., Drezner M. K. Calcification of entheses associated with X‐linked hypophosphatemic osteomalacia. N Engl J Med 1985; 313(1)1–6
  • Stickler G. B., Beabout J. W., Riggs B. L. Vitamin D‐resistant rickets: clinical experience with 41 typical familial hypophosphatemic patients and 2 atypical nonfamilial cases. Mayo Clin Proc 1970; 45(3)197–218
  • Winters R. W., Graham J. B., Williams T. F., McFalls V. W., Burnett C. H. A genetic study of familial hypophosphatasia and vitamin D‐resistant rickets, with a review of the literature. Medicine 1958; 37: 97–142

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