Serveur d'exploration sur le patient édenté (maquette)

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

Identifieur interne : 000589 ( PubMed/Curation ); précédent : 000588; suivant : 000590

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

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pubmed:23484169

Le document en format XML

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<title xml:lang="en">Brånemark system implants and rare disorders: a report of six cases.</title>
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<nlm:affiliation>The Brånemark Clinic, Clinic of Odontology, Göteborg, Sweden. bertil.friberg@vgregion.se</nlm:affiliation>
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<term>Dental Implantation, Endosseous (methods)</term>
<term>Dental Implants</term>
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<term>Dentinogenesis Imperfecta (complications)</term>
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<term>Histiocytose à cellules de Langerhans ()</term>
<term>Humains</term>
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<term>Planification des soins du patient</term>
<term>Pose d'implant dentaire endo-osseux ()</term>
<term>Prothèse dentaire implanto-portée</term>
<term>Prémolaire (anatomopathologie)</term>
<term>Rachitisme hypophosphatémique familial ()</term>
<term>Résorption alvéolaire ()</term>
<term>Résultat thérapeutique</term>
<term>Études de suivi</term>
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<term>Canine</term>
<term>Incisive</term>
<term>Molaire</term>
<term>Prémolaire</term>
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<term>Dentinogenesis Imperfecta</term>
<term>Familial Hypophosphatemic Rickets</term>
<term>Histiocytosis, Langerhans-Cell</term>
<term>Osteogenesis Imperfecta</term>
<term>Periodontal Diseases</term>
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<term>Dental Implantation, Endosseous</term>
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<term>Bicuspid</term>
<term>Cuspid</term>
<term>Incisor</term>
<term>Molar</term>
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<term>Treatment Outcome</term>
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<term>Adulte d'âge moyen</term>
<term>Dentinogenèse imparfaite</term>
<term>Femelle</term>
<term>Histiocytose à cellules de Langerhans</term>
<term>Humains</term>
<term>Implants dentaires</term>
<term>Jeune adulte</term>
<term>Maladies parodontales</term>
<term>Maladies rares</term>
<term>Mâle</term>
<term>Ostéogenèse imparfaite</term>
<term>Planification des soins du patient</term>
<term>Pose d'implant dentaire endo-osseux</term>
<term>Prothèse dentaire implanto-portée</term>
<term>Rachitisme hypophosphatémique familial</term>
<term>Résorption alvéolaire</term>
<term>Résultat thérapeutique</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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