Karabagli, Pinar2020-03-262020-03-2620130256-70401433-0350https://dx.doi.org/10.1007/s00381-013-2284-4https://hdl.handle.net/20.500.12395/29713Premature closure and subsequent ossification of the metopic suture results in triangular head shape called trigonocephaly and is characterized by a midline metopic ridge, frontotemporal narrowing, and an increased biparietal diameter. Trigonocephaly is the second most frequent type of craniosynostosis. It can be isolated and associated with other congenital anomalies without any known syndrome, or occurs as part of a multiple malformation syndrome. Improvement in treatment is directed by a thorough understanding of the basic pathology of this condition. This review aims to provide an overview of metopic synostosis by correlating what is known about pathogenesis and pathology of this entity.en10.1007/s00381-013-2284-4info:eu-repo/semantics/closedAccessTrigonocephalyMetopic suturePathologyCraniosynostosisPathology in metopic synostosisArticle29122165217024092422Q2WOS:000327894900007Q3