Variable prenatal presentation of Pfeiffer syndrome: Suggested aids to prenatal sonographic diagnosis.
Souha SalibaBaptiste MorelMarie GonzalesMarie-Victoire SénatLucie GuilbaudJean-Marie JouannicMarie CassartCatherine GarelEléonore BlondiauxPublished in: Prenatal diagnosis (2018)
Pfeiffer syndrome has a highly variable phenotype, and the absence of craniosynostosis on prenatal US does not exclude the diagnosis. Presence of abnormal thumbs and big toes, a sacral appendage, vertebral fusions, and coronal clefts should lead to prenatal molecular testing for PS.