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 2024/10/07 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.