Pyknodysostosis: A rare case report

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...

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Veröffentlicht in:Journal of Indian Academy of Oral Medicine and Radiology 2015-04, Vol.27 (2), p.318-321
Hauptverfasser: Bhardwaj, Deepti, Raghav, Namita, Mohan, Vinay, Singh, Pooja
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Sprache:eng
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Zusammenfassung: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.
ISSN:0972-1363
0975-1572
DOI:10.4103/0972-1363.170175