Pre- and postnatal imaging of Pai syndrome with spontaneous intrauterine closure of a frontal cephalocele.

Dobrocky, TomasTomasDobrockyEbner, LukasLukasEbnerLiniger, BenjaminBenjaminLinigerWeisstanner, ChristianChristianWeisstannerStranzinger, EnnoEnnoStranzinger2024-10-232024-10-232015-06https://boris-portal.unibe.ch/handle/20.500.12422/128426Pai syndrome is a rare congenital disorder characterized by cutaneous polyps of the face, pericallosal lipoma and median cleft lip. We report on a newborn girl with a variant of Pai syndrome presenting with all typical findings except a median cleft. In addition, fetal sonography and MRI showed the unique intrauterine evolution of a cephalocele into an atretic cephalocele.en600 - Technology::610 - Medicine & healthPre- and postnatal imaging of Pai syndrome with spontaneous intrauterine closure of a frontal cephalocele.article10.7892/boris.618532535943310.1007/s00247-014-3205-8