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
Lingua originale | Italian |
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pagine (da-a) | 304-306 |
Numero di pagine | 3 |
Rivista | Recenti Progressi in Medicina |
Volume | 100 |
Stato di pubblicazione | Published - 2009 |
All Science Journal Classification (ASJC) codes
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