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Osteomyelitis in Pycnodysostosis – Report of 2 Clinical Cases

Identifieur interne : 005911 ( Ncbi/Checkpoint ); précédent : 005910; suivant : 005912

Osteomyelitis in Pycnodysostosis – Report of 2 Clinical Cases

Auteurs : Rohit S. ; Praveen Reddy B. ; Sreedevi B. ; Sandeep Prakash

Source :

RBID : PMC:4347182

Abstract

Pycnodysostosis is a rare craniofacial syndrome characterized by dwarfism, cranial anomalies, diffuse osteosclerosis where multiple fracture of long bones and osteomyelitis of jaw are frequent complications. This clinical entity was first described in 1962 by Maroteaux and Lamy. This article presents two clinical cases of pycnodysostosis with their clinical and radiological characteristics.


Url:
DOI: 10.7860/JCDR/2015/10114.5461
PubMed: 25738091
PubMed Central: 4347182


Affiliations:


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PMC:4347182

Le document en format XML

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<p>Pycnodysostosis is a rare craniofacial syndrome characterized by dwarfism, cranial anomalies, diffuse osteosclerosis where multiple fracture of long bones and osteomyelitis of jaw are frequent complications. This clinical entity was first described in 1962 by Maroteaux and Lamy. This article presents two clinical cases of pycnodysostosis with their clinical and radiological characteristics.</p>
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