TY  - CHAP
M1  - Book, Section
TI  - Encephalocele
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
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).  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/18
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=1164068926
ER  -