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Pycnodysostosis: A bone dysplasia with unusual oral manifestation
Pycnodysostosis, a sclerosing bone dysplasia, is a rare autosomal recessive disorder with an estimated prevalence rate of one in one million. Patients with pycnodyostosis usually have normal intelligence, sexual development and life span. This condition is characterized by increased bone density and...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260389/ https://www.ncbi.nlm.nih.gov/pubmed/25565757 http://dx.doi.org/10.4103/0975-962X.144738 |
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author | Balaji, M S Anandi Sundaram, R Kanmani Shanmuga Karthik, Poornima Asokan, Kannan |
author_facet | Balaji, M S Anandi Sundaram, R Kanmani Shanmuga Karthik, Poornima Asokan, Kannan |
author_sort | Balaji, M S Anandi |
collection | PubMed |
description | Pycnodysostosis, a sclerosing bone dysplasia, is a rare autosomal recessive disorder with an estimated prevalence rate of one in one million. Patients with pycnodyostosis usually have normal intelligence, sexual development and life span. This condition is characterized by increased bone density and fragility along with oral manifestations like malposition teeth, hypoplastic maxilla, receded chin and delayed eruption of permanent teeth with discharging sinuses in the jaws because of poor blood supply. This is one such rare case report of a 47-year-old patient presenting with a complaint of fractured jaw and reviewing the clinical and radiographic characteristics of pycnodysostosis. |
format | Online Article Text |
id | pubmed-4260389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42603892014-12-22 Pycnodysostosis: A bone dysplasia with unusual oral manifestation Balaji, M S Anandi Sundaram, R Kanmani Shanmuga Karthik, Poornima Asokan, Kannan Indian J Dent Case Report Pycnodysostosis, a sclerosing bone dysplasia, is a rare autosomal recessive disorder with an estimated prevalence rate of one in one million. Patients with pycnodyostosis usually have normal intelligence, sexual development and life span. This condition is characterized by increased bone density and fragility along with oral manifestations like malposition teeth, hypoplastic maxilla, receded chin and delayed eruption of permanent teeth with discharging sinuses in the jaws because of poor blood supply. This is one such rare case report of a 47-year-old patient presenting with a complaint of fractured jaw and reviewing the clinical and radiographic characteristics of pycnodysostosis. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4260389/ /pubmed/25565757 http://dx.doi.org/10.4103/0975-962X.144738 Text en Copyright: © Indian Journal of Dentistry http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Balaji, M S Anandi Sundaram, R Kanmani Shanmuga Karthik, Poornima Asokan, Kannan Pycnodysostosis: A bone dysplasia with unusual oral manifestation |
title | Pycnodysostosis: A bone dysplasia with unusual oral manifestation |
title_full | Pycnodysostosis: A bone dysplasia with unusual oral manifestation |
title_fullStr | Pycnodysostosis: A bone dysplasia with unusual oral manifestation |
title_full_unstemmed | Pycnodysostosis: A bone dysplasia with unusual oral manifestation |
title_short | Pycnodysostosis: A bone dysplasia with unusual oral manifestation |
title_sort | pycnodysostosis: a bone dysplasia with unusual oral manifestation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260389/ https://www.ncbi.nlm.nih.gov/pubmed/25565757 http://dx.doi.org/10.4103/0975-962X.144738 |
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