Oral findings in Rett syndrome : a systematic review of the dental literature
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Oral findings in Rett syndrome : a systematic review of the dental literature

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Oral findings in Rett syndrome : a systematic review of the dental literature

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Fuertes González, María Cristina; Silvestre Donat, Francisco Javier; Almerich Silla, José Manuel Perfil
Aquest document és un/a article publicat, creat/da en: 2011
Rett syndrome (RS) is a chromosome X-linked genetic neurological disorder characterized by developmental regression, particularly in relation to expressive language and use of the hands, together with profound mental retardation, that almost exclusively affects females. The present review describes the 35 cases of RS Publisher in the indexed literature (Medline) ? the first corresponding to 1985 and the last to the year 2007. Certain oral manifestations of the disease are derived from the drug treatment prescribed to control the disease, while others are common to other clinical conditions characterized by convulsion activity, difficulties for correct oral hygiene, walking problems and/or an excess of oral / digital-manual habits. In any case, bruxism is the oral habit most frequently associated with RS ? the treatment of which remains the subject of controversy.

    Fuertes González, María Cristina ; Silvestre Donat, Francisco Javier ; Almerich Silla, José Manuel. Oral findings in Rett syndrome : a systematic review of the dental literature. En: Medicina oral, patología oral y cirugía bucal. Ed. inglesa, 16 1 2011: 9-
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