Rett syndrome affects one in every 10,000 15,000 liveborn female babies in all racial and ethnic groups worldwide. Informatiemateriaal nederlandse rett syndroom vereniging. Il fait partie des troubles envahissants du developpement ted. E una patologia ad insorgenza tardiva intorno ai 18. Lenfant, dont le developpement etait normal, diminue son interet pour les jouets ou les personnes. Complications can include seizures, scoliosis, and sleeping problems. Catalog home health topics rett syndrome rett syndrome 2 products local navigation. Feb 27, 2019 please use one of the following formats to cite this article in your essay, paper or report. Goidstein, md nine girls with rett syndrome had 22 electroen cephalographic studies performed over 5 years. Sindrome di rett, subiscono una notevole regressione nello sviluppo hagberg, 1993. This article is focus on the currently knowledge about rett syndrome, based on the more recent information in the international literature on genetic and epidemiological aspects of this condition, as well as on its clinical and.
It is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability. Rett syndrome in girls is characterized by a serious and global developmental disorder affecting the. Often there is slower growth, problems walking, and a smaller head size. Pdf rett syndrome rtt is a neurological disorder caused by mutations in the xlinked gene methylcpgbinding protein 2 mecp2. Pineda m, aracil a, vernet a, espada m, cobo e, arteaga. Eeg abnormalities aid diagnosis of rett syndrome elizabeth a. Les petites filles malades ont une deficience intellectuelle severe et presentent des complications multiples, dont des troubles respiratoires et cardiovasculaires. Pdf rett syndrome rtt is a profound neurodevelopmental disorder that primarily affects females resulting in severe intellectual and physical. Nine teen waking tracings demonstrated moderate back ground slowing. O sexo feminino e atingido numa prevalencia estimada entre 1. Mar 25, 2015 rett syndrome affects one in every 10,000 15,000 liveborn female babies in all racial and ethnic groups worldwide. Rett syndrome is a rare, severe neurological disorder that affects mostly girls.
Symptoms include problems with language, coordination, and repetitive movements. Since the disorder usually occurs spontaneously, there is less than a 1% risk of another child in the same family being born with rett syndrome. Patients with rett syndrome should be seen for regular wellness checkups, screenings and immunizations especially flu vaccinations. Rett syndrome rett syndrome is a neurologicalmovement disorder which predominantly affects girls approximately 1 in 10,000. Soriano fonseca f, aguilar rebolledo f, morales hernandez e. Aandachtspunten voor mensen met het rett syndroom kennisplein. Its usually discovered in the first two years of life, and a childs diagnosis with rett syndrome can feel. Rett syndrome rtt is a genetic brain disorder that typically becomes apparent after 6 to 18 months of age in females. Rett syndrome is a neurodevelopmental disorder that affects girls almost exclusively. In 1983, rett syndrome was recognized as a known condition and much more research was to follow including the determination and publication of a set of diagnostic criteria.