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Compend Contin Educ Dent ; 35(2): e6-11, 2014 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24571544

RESUMO

This report describes the treatment of a young male patient diagnosed with amelogenesis imperfecta (AI), a hereditary disorder that affects the enamel of both primary and permanent dentition. For management and rehabilitation, it is crucial to determine the type of AI-hypoplastic, hypomaturation, or hypocalcified. As with this patient, who presented with tricho-dento osseous syndrome, patients may present with associated expression of a syndrome (partial or full) and secondary changes in the periodontium. AI is a serious problem; therefore extensive treatment using a multidisciplinary approach must be instituted, especially if the patient is syndrome-associated.


Assuntos
Amelogênese Imperfeita/terapia , Restauração Dentária Permanente , Doenças Periodontais/terapia , Adolescente , Amelogênese Imperfeita/diagnóstico , Prótese Dentária , Humanos , Masculino
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