Pseudomelia paresthetica syndrome (Syndrome of Pseudomelia Paarsthetica) is a rare genetic disease that is characterized by asymmetric deformation of the limbs and trunk, as well as impaired skin sensitivity. A characteristic feature of the syndrome is the “bifurcation” of the torso, which leads to the appearance of two separate parts of the body. This occurs due to impaired development of the nervous system and spine. Pseudomalia paresthetic syndrome in a child manifests itself from birth to the third year of life. It can be caused by both hereditary factors and certain external conditions. There is no specific treatment for the disease, but proper diagnosis and appropriate treatment can help reduce the severity