Klc syndrome

**KL syndrome** is a genetically determined developmental disorder: premature closure of the forebrain of the fetal head, leading to various abnormalities of the nervous system and skeleton. In the literature, this term is assigned to a certain nosological form of one of the forms of facial anomaly, dysontogenesis of the central nervous system. There is another version, according to which KL syndrome is a disease characterized by one symptom. Bony curvature of the head, receding chin, funnel chest