Rett syndrome is a rare genetic disorder that affects the way the brain develops. It occurs almost exclusively in baby girls. Most of the children with Rett syndrome seem to develop normally at first, but symptoms external after 6 months of age. Supplementary, children with Rett syndrome have increasing problems with movement, coordination and communication that may affect their ability to use their hands, communicate and walk.
Related Journals of Rett syndrome
Journal of Medical Genetics, Human Molecular Genetics, Orphanet Journal of Rare Diseases, Journal of Neurodevelopmental Disorders, Journal of Child Neurology, European Journal of Human Genetics, The Journal of Neuroscience, International Journal of Developmental Neuroscience, Journal of Pediatric Neurology, Frontiers in Cellular Neuroscience.