RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164068437
T1 Duker Weiss Siber 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=1164068437
RD 2024/04/23
AB It  is  a  genetic  disorder  that  affects  mainly  males  and  characterized  by  ocular  anomalies  (eg,  microphthalmos),  microencephaly,  mental  retardation,  agenesis  of  the  corpus  callosum,  and  urogenital  anomalies.  This  medical  condition  is  lethal  in  infancy.