TY  - CHAP
M1  - Book, Section
TI  - Donnai-Barrow Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
Y1  - 2019
N1  - 
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - It  is  a  genetic  disorder  characterized  by  the  association  of  diaphragmatic  hernia,  exomphalos,  absent  corpus  callosum,  hypertelorism,  eye  anomalies,  and  sensorineural  deafness.  The  classic  distinguishing  features  between  faciooculoacousticorenal  (FOAR)  and  Donnai-Barrow  Syndromes  are  the  presence  of  proteinuria,  the  absence  of  diaphragmatic  hernia  and  agenesis  of  the  corpus  callosum  in  the  FOAR  Syndrome.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/18
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164068200
ER  -