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Brånemark system implants and rare disorders: a report of six cases.

Identifieur interne : 011614 ( Main/Exploration ); précédent : 011613; suivant : 011615

Brånemark system implants and rare disorders: a report of six cases.

Auteurs : Bertil Friberg [Suède]

Source :

RBID : pubmed:23484169

Descripteurs français

English descriptors

Abstract

Rare disorders are conditions defined as either fatal or causing chronic functional impairment. There is limited evidence of the behavior of oral implants in patients suffering from such diseases, and the existing data are merely based on cases reports. This paper describes the outcome of implant treatment after up to 15 years of function in three patients afflicted with X-linked hypophosphatemia, two patients with Langerhans cell histiocytosis, and one patient with osteogenesis/dentinogenesis imperfecta.

PubMed: 23484169


Affiliations:


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Le document en format XML

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<term>Dental Implantation, Endosseous (methods)</term>
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<term>Dental Prosthesis, Implant-Supported</term>
<term>Dentinogenesis Imperfecta (complications)</term>
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<term>Canine (anatomopathologie)</term>
<term>Dentinogenèse imparfaite ()</term>
<term>Femelle</term>
<term>Histiocytose à cellules de Langerhans ()</term>
<term>Humains</term>
<term>Implants dentaires</term>
<term>Incisive (anatomopathologie)</term>
<term>Jeune adulte</term>
<term>Maladies parodontales ()</term>
<term>Maladies rares</term>
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<term>Pose d'implant dentaire endo-osseux ()</term>
<term>Prothèse dentaire implanto-portée</term>
<term>Prémolaire (anatomopathologie)</term>
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<div type="abstract" xml:lang="en">Rare disorders are conditions defined as either fatal or causing chronic functional impairment. There is limited evidence of the behavior of oral implants in patients suffering from such diseases, and the existing data are merely based on cases reports. This paper describes the outcome of implant treatment after up to 15 years of function in three patients afflicted with X-linked hypophosphatemia, two patients with Langerhans cell histiocytosis, and one patient with osteogenesis/dentinogenesis imperfecta.</div>
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