Literature DB >> 18974541

Pyknodysostosis: oral findings and differential diagnosis.

L F Soares1, I P R Souza, A S Cardoso, L Pomarico.   

Abstract

Pyknodysostosis is a rare, genetic, autosomal recessive condition characterized by short stature, generalized bone sclerosis, and oral manifestations such as maxillary atresia and an increase of the mandibular angle. The main purpose of this article was to report a case of pyknodysostosis, describing the characteristic orofacial findings of the disease and discussing the differential diagnosis.

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Year:  2008        PMID: 18974541

Source DB:  PubMed          Journal:  J Indian Soc Pedod Prev Dent        ISSN: 0970-4388


  3 in total

Review 1.  Clinical and radiographic maxillofacial features of pycnodysostosis.

Authors:  Nilton Alves; Mario Cantín
Journal:  Int J Clin Exp Med       Date:  2014-03-15

Review 2.  Clinical and animal research findings in pycnodysostosis and gene mutations of cathepsin K from 1996 to 2011.

Authors:  Yang Xue; Tao Cai; Songtao Shi; Weiguang Wang; Yanli Zhang; Tianqiu Mao; Xiaohong Duan
Journal:  Orphanet J Rare Dis       Date:  2011-05-10       Impact factor: 4.123

3.  Pyknodysostosis: report of a rare case with review of literature.

Authors:  Kiran Kumar Kotagudda Ramaiah; Giju Baby George; Sheeba Padiyath; Rupak Sethuraman; Babu Cherian
Journal:  Imaging Sci Dent       Date:  2011-12-19
  3 in total

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