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Infantile osteopetrosis associated with osteomyelitis

Identifieur interne : 001A28 ( Pmc/Corpus ); précédent : 001A27; suivant : 001A29

Infantile osteopetrosis associated with osteomyelitis

Auteurs : Cintia De Vasconcellos Machado ; Maria Celina Barreiros Siquara Da Rocha ; Paloma Dias Da Silva Telles

Source :

RBID : PMC:4369041

Abstract

Osteopetrosis is a rare inherited disorder characterised by the inability to reabsorb and remodel bone due to an osteoclast dysfunction. An increase in bone mass and density results in severe skeletal malformation and bone marrow failure, which may be fatal. The aim of this study was to report a case of infantile osteopetrosis in a 6-year-old boy, who primarily complained of dental problems. The patient developed an osteomyelitis after a primary tooth extraction. We also reviewed the literature about this genetic bone disease, since the management of dental problems of these patients can be a challenge to the dentist. The diagnosis, clinical and radiographic features and treatment of the case were discussed in this work.


Url:
DOI: 10.1136/bcr-2014-208085
PubMed: 25743862
PubMed Central: 4369041

Links to Exploration step

PMC:4369041

Le document en format XML

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<addr-line>Childhood Pediatric Clinic</addr-line>
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<name sortKey="Siquara Da Rocha, Maria Celina Barreiros" sort="Siquara Da Rocha, Maria Celina Barreiros" uniqKey="Siquara Da Rocha M" first="Maria Celina Barreiros" last="Siquara Da Rocha">Maria Celina Barreiros Siquara Da Rocha</name>
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<name sortKey="Telles, Paloma Dias Da Silva" sort="Telles, Paloma Dias Da Silva" uniqKey="Telles P" first="Paloma Dias Da Silva" last="Telles">Paloma Dias Da Silva Telles</name>
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<addr-line>Department of Social and Pediatric Dentistry</addr-line>
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<p>Osteopetrosis is a rare inherited disorder characterised by the inability to reabsorb and remodel bone due to an osteoclast dysfunction. An increase in bone mass and density results in severe skeletal malformation and bone marrow failure, which may be fatal. The aim of this study was to report a case of infantile osteopetrosis in a 6-year-old boy, who primarily complained of dental problems. The patient developed an osteomyelitis after a primary tooth extraction. We also reviewed the literature about this genetic bone disease, since the management of dental problems of these patients can be a challenge to the dentist. The diagnosis, clinical and radiographic features and treatment of the case were discussed in this work.</p>
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Professor Cintia de Vasconcellos Machado,
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<p>Osteopetrosis is a rare inherited disorder characterised by the inability to reabsorb and remodel bone due to an osteoclast dysfunction. An increase in bone mass and density results in severe skeletal malformation and bone marrow failure, which may be fatal. The aim of this study was to report a case of infantile osteopetrosis in a 6-year-old boy, who primarily complained of dental problems. The patient developed an osteomyelitis after a primary tooth extraction. We also reviewed the literature about this genetic bone disease, since the management of dental problems of these patients can be a challenge to the dentist. The diagnosis, clinical and radiographic features and treatment of the case were discussed in this work.</p>
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