A rare congenital disorder characterized by multiple malformations, including specific facial features, growth retardation, skeletal abnormalities, and intellectual disabilities. Possible manifestations include microcephaly, cleft palate, limb abnormalities and various defects of internal organs, but the clinical picture can vary significantly from patient to patient. It is believed to be genetic in nature, but the exact cause and type of inheritance have not been established due to the extremely small number of cases described. Treatment is supportive and aimed at correcting individual symptoms with the participation of specialists in various fields.