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Dental management in autosomal recessive (intermediate) osteopetrosis: a case report.

Identifieur interne : 011467 ( Main/Exploration ); précédent : 011466; suivant : 011468

Dental management in autosomal recessive (intermediate) osteopetrosis: a case report.

Auteurs : Vishal Bansal [Inde] ; Sanjeev Kumar ; K V Arunkumar ; Apoorva Mowar ; Gagan Khare

Source :

RBID : pubmed:21462770

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English descriptors

Abstract

Osteopetrosis (Albers-Schonberg disease) is the name given to a group of diseases that affect the growth and remodeling of bones. It is characterized by overgrowth and sclerosis of bone, resulting in thickening and narrowing of the marrow cavities throughout the skeleton. The exact cause is unknown, although failure of bone resorption related to defective osteoclasts is considered to be the basis of the problem. These patients present a significant challenge to the dentist for management of jaw and dental problems, as the disease process demands special strategies which are often at variance with conventional dentistry. The purpose of this paper was to report the management and follow-up of a child with intermediate autosomal recessive osteopetrosis who primarily complained of dental problems.

PubMed: 21462770


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Le document en format XML

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<nlm:affiliation>Department of Oral and Maxillofacial Surgery, Subharti Dental College and Hospital, Meerut, Uttar Pradesh, India. drbansalvishal@rediffmail.com</nlm:affiliation>
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<term>Adolescent</term>
<term>Dental Care for Chronically Ill (methods)</term>
<term>Denture Design</term>
<term>Denture, Complete</term>
<term>Female</term>
<term>Humans</term>
<term>Jaw, Edentulous, Partially (complications)</term>
<term>Jaw, Edentulous, Partially (diagnostic imaging)</term>
<term>Jaw, Edentulous, Partially (rehabilitation)</term>
<term>Jaw, Edentulous, Partially (surgery)</term>
<term>Mandibular Diseases (complications)</term>
<term>Mandibular Diseases (diagnostic imaging)</term>
<term>Mandibular Diseases (surgery)</term>
<term>Osteomyelitis (etiology)</term>
<term>Osteomyelitis (therapy)</term>
<term>Osteopetrosis (complications)</term>
<term>Osteopetrosis (genetics)</term>
<term>Osteopetrosis (therapy)</term>
<term>Radiography</term>
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<term>Tooth, Unerupted (etiology)</term>
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<term>Dent incluse (imagerie diagnostique)</term>
<term>Dent incluse (étiologie)</term>
<term>Femelle</term>
<term>Humains</term>
<term>Maladies mandibulaires ()</term>
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<term>Mâchoire partiellement édentée ()</term>
<term>Mâchoire partiellement édentée (imagerie diagnostique)</term>
<term>Mâchoire partiellement édentée (rééducation et réadaptation)</term>
<term>Ostéomyélite ()</term>
<term>Ostéomyélite (étiologie)</term>
<term>Ostéopétrose ()</term>
<term>Ostéopétrose (génétique)</term>
<term>Prothèse dentaire complète</term>
<term>Radiographie</term>
<term>Soins dentaires pour malades chroniques ()</term>
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<term>Jaw, Edentulous, Partially</term>
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<term>Dent incluse</term>
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<term>Mâchoire partiellement édentée</term>
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<term>Maladies mandibulaires</term>
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<front>
<div type="abstract" xml:lang="en">Osteopetrosis (Albers-Schonberg disease) is the name given to a group of diseases that affect the growth and remodeling of bones. It is characterized by overgrowth and sclerosis of bone, resulting in thickening and narrowing of the marrow cavities throughout the skeleton. The exact cause is unknown, although failure of bone resorption related to defective osteoclasts is considered to be the basis of the problem. These patients present a significant challenge to the dentist for management of jaw and dental problems, as the disease process demands special strategies which are often at variance with conventional dentistry. The purpose of this paper was to report the management and follow-up of a child with intermediate autosomal recessive osteopetrosis who primarily complained of dental problems.</div>
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<name sortKey="Kumar, Sanjeev" sort="Kumar, Sanjeev" uniqKey="Kumar S" first="Sanjeev" last="Kumar">Sanjeev Kumar</name>
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