Journal of Indian Academy of Oral Medicine and Radiology (Jan 2015)

Pyknodysostosis: A rare case report

  • Deepti Bhardwaj,
  • Namita Raghav,
  • Vinay Mohan,
  • Pooja Singh

DOI
https://doi.org/10.4103/0972-1363.170175
Journal volume & issue
Vol. 27, no. 2
pp. 318 – 321

Abstract

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Pyknodysostosis is a rare autosomal recessive disorder characterized by the postnatal onset of short limbs, short stature, and generalized hyperostosis along with acro-osteolysis with sclerosis of the terminal phalanges, a feature that is considered essentially pathognomonic. Other features include persistence of fontanelles, delayed closure of sutures, wormian bones, absence of frontal sinuses, and obtuse mandibular gonial angle with relative mandibular prognathism. Here, we report a case of pyknodysostosis found to be having the classical features during intraoral examination and general physical examination.

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