[Functional and occlusion rehabilitation in a patient with Rett syndrome: a case report]

Recenti Prog Med. 2009 Jun;100(6):304-6.
[Article in Italian]

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.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Child
  • Female
  • Humans
  • Orthodontic Appliances*
  • Rett Syndrome / rehabilitation*