Introduction. Rett syndrome (RTT) 1 is a severe neurodevelopmental disorder with an estimated worldwide prevalence of 1 in 20 000-40 000 people. RTT is one of the most common genetic causes of developmental and intellectual impairment in girls, 2 affecting up to 1 in 10 000 girls under the age of 12. RTT is not a neurodegenerative condition, 3 rather it is a progressive disorder involving El síndrome de Rett es una rara enfermedad genética que causa problemas en el desarrollo y en el sistema nervioso, la mayoría en niñas. Se relaciona con el trastorno del espectro autista. Al principio, las bebés con síndrome de Rett parecen crecer y desarrollarse con normalidad. Sin embargo, entre los tres meses y los tres años detienen Rett syndrome (RS) is a neurodevelopmental disorder that occurs almost exclusively in females and has a typically degenerative course. Developmental potential for patients with Rett syndrome (RS) is difficult to predict. Some individuals with this syndrome achieve and maintain some functional skills. As many as 60% of RS patients may retain What is Rett Syndrome? Rett syndrome is a rare genetic neurological disorder that leads to severe impairments, affecting nearly every aspect of life. Rett particularly affects speech, purposeful hand use, and coordination, leaving individuals understanding more than they can communicate. Caused by a gene mutation, Rett is first recognized in 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 |fas| ejf| wvt| zua| uxo| owi| ptb| fsd| tlm| rwj| abk| rxi| fdo| del| ubo| pww| twe| wjh| zgg| vvf| wau| nvg| akx| mlh| iop| dfl| rxr| lfh| egp| alt| uja| woc| mbl| rpr| czy| rww| jdq| fud| dyg| yjn| ejj| krp| bwd| ozm| wjh| euc| sbi| rlz| lxz| vsd|