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GIUSEPPA BILELLO

Riequilibrio occluso-funzionale in un soggetto con sindrome di Rett: descrizione di un caso

Abstract

Rett syndrome is a severe neurodevelopmental disease caused by mutations in the X-linked gene encoding for the methyl-CpG-binding protein MeCP2. The aim of this paper is to show the orthodontic treatment of a little girls affected by Rett syndrome