Little Matyas (2) has the serious genetic disease Rett syndrome. They do not feel pain, the parents are asking the public for help

Rett syndrome is a serious neurological disease that mainly affects girls. However, it also rarely occurs in boys, where the symptoms are often more severe. The case of little Matyas from Brankovice in the Vyškov region is one of these rare cases. Matyas, who is almost three years old, was diagnosed with this disease, which significantly complicates his life and the life of his family. Genetics and manifestations of Rett syndrome: Rett syndrome is caused by a mutation on the X chromosome and is usually manifested by a gradual deterioration of motor functions and mental abilities.