Paroxysmal Janeway-Mosenthal syndrome

Janeway-Mosenthal syndrome (JMS) is a rare hereditary disease in children in which the patient develops various abnormalities of physical development. PCD has two forms: with and without skull deformation. Moreover, both forms of PZD can manifest themselves in the same family in different generations and by chance. In 2021, only three cases of detection of multiple forms of J syndrome were registered worldwide.