Pyknodysostosis: Imaging and laboratory observations

S. Karkabi, N. D. Reis, S. Linn, G. Edelson, E. Tzehoval, V. Zakut, E. Dolev, E. Bar-Meir, S. Ish-Shalom

Research output: Contribution to journalArticlepeer-review


Pyknodysostosis is a rare form of sclerosing bone dysplasia with autosomal recessive inheritance. Affected members of two families were assessed as follows: three patients underwent densitometry measurements and bone scans; four patients underwent magnetic resonance imaging (MRI) and an immunological investigation, as well as a detailed endocrinological and biochemical laboratory review. Densitometry measurements revealed values of up to 291% of age-matched normal controls; this increased bone density was mainly in the trabecular bone and not in the cortical bone. The MRI showed the cortex to be of normal thickness, whereas the increase in trabecular bone limited the space within the medullary canal. Bone scans and single photon emission computerized tomography in three patients showed an increased uptake of [99mTc]methylene diphosphonate of up to 538% of age-matched controls, which reflected the increased bone density. Monocyte function tests demonstrated a normal phagocytic capacity, but their killing activity was impaired. Interleukin-1 secretion was also impaired, which may point to the pathogenesis of the disease, in view of its function as an osteoclast activator and its role in bone resorption.

Original languageEnglish
Pages (from-to)170-173
Number of pages4
JournalCalcified Tissue International
Issue number3
StatePublished - Sep 1993
Externally publishedYes


  • Interleukin-1
  • MRI
  • Monocyte function tests
  • Pyknodysostosis

ASJC Scopus subject areas

  • Endocrinology
  • Endocrinology, Diabetes and Metabolism
  • Orthopedics and Sports Medicine


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