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lüll Particularites cliniques du syndrome de Rett Abbes Z; Bouden A; Halayem S; Othman S; Bechir Halayem MTunis Med 2011[Oct]; 89 (10): 733-7BACKGROUND: Rett Syndrome is a neurodevelopmental disorder, one of the least commonly occurring autism spectrum disorders (ASD),affecting mainly females. AIM: To describe features and molecular specificities of Rett syndrome. METHODS: To identify articles for this review, a Pubmed search was conducted using the following keywords: Rett syndrome, regression,mutation, stereotypes. RESULTS: This syndrome is characterized by cognitive impairment,communication dysfunction, stereotypic movement disorder, and growth failure. It is generally caused by mutations in the MECP2 gene. Rett Syndrome has a prevalence ranging from 10-20 000 females. Specific treatment is not available, but patients need a careful planning for long-term care, with multidisciplinary approaches.|Diagnosis, Differential[MESH]|Humans[MESH]|Prognosis[MESH]|Rett Syndrome/*diagnosis/genetics[MESH] |