Rett syndrome is an uncommon neurological condition that affects mostly girls. Developmental difficulties, loss of motor abilities, and speech are all symptoms of the condition. Furthermore, the syndrome is diagnosed in children aged 6 to 18 months and is caused by mutations in the MECP2 gene on the X-chromosome. Rett syndrome can cause various problems, ranging from moderate to severe. Unusual eye movements, delayed growth, agitation and anger, poor language abilities, hand movement problems, muscular and coordination challenges, and breathing problems are all common symptoms of Rett syndrome.
