RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164068200
T1 Donnai-Barrow Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accesspediatrics.mhmedical.com/content.aspx?aid=1164068200
RD 2021/01/22
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.