RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164068926 T1 Encephalocele T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164068926 RD 2024/03/29 AB Malformation characterized by cerebral anomalies and a median skull gap originating from the nasal root, orbits, or forehead (sincipital encephalocele), or the skull base or occiput (occipital encephalocele), allowing cerebrospinal fluid and/or brain to herniate. The encephalocele itself is defined as a herniation of part of the cranial contents through this skull defect. It may contain meninges (meningocele), meninges and brain (meningoencephalocele), or meninges, brain, and ventricle (meningoencephalocystocele).