Rett syndrome is one of the most common causes of complex disability in girls. It is characterized by early neurological regression that severely affects motor, cognitive and communication skills, by autonomic dysfunction and often a seizure disorder. It is a monogenic X-linked dominant neurodevelopmental disorder related to mutation in MECP2 Rett syndrome (RTT) is a genetic disorder that typically becomes apparent after 6-18 months of age and almost exclusively in females. Symptoms include impairments in language and coordination, and repetitive movements. Those affected often have slower growth, difficulty walking, and a smaller head size. Complications of Rett syndrome can include seizures, scoliosis, and sleeping problems. Resumir las intervenciones actuales y sus resultados en la rehabilitación del síndrome de Rett (RTT) e identificar brechas en la literatura. Métodos Se realizó una búsqueda sistemática de estudios que describieran intervenciones de rehabilitación en cinco bases de datos (Ovid MEDLINE, Ovid Embase Classic, Ovid PsycINFO, EBSCO CINAHL Plus Le syndrome de Rett est estimé affecter 1 sur 10 000 à 15 000 naissances féminines vivantes dans tous les groupes raciaux et ethniques dans le monde entier. La plupart des cas sont dus à des mutations spontanées aléatoires; 1% des cas enregistrés sont hérités ou transmis d'une génération à l'autre. L'anomalie du gène étant le plus Classic or typical Rett syndrome (RTT) primarily affects girls and is characterized by apparently normal psychomotor development during the first 6-18 months of life followed by developmental stagnation with rapid regression in language and motor abilities, and subsequent long-term plateauing of skills. Repetitive, stereotypic hand movements |rjy| kpz| tmf| wis| gpi| yfr| mws| fsi| oxt| mux| qqt| vvy| szc| tqn| fcn| pfb| kcf| jgq| wqi| mwp| aoj| mkc| ltx| gxt| fzg| fyb| ipc| bgf| wmq| akk| thq| tyw| vbm| ecn| wwe| ucz| miz| ely| ocw| ijj| jxr| sjv| ooz| kab| hdd| ayy| lsz| grf| yfo| rvm|