RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164075894 T1 Krause-van Schooneveld-Kivlin 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=1164075894 RD 2024/03/29 AB This congenital medical condition is characterized by the combination of short limb dwarfism, facial anomalies, and mental retardation with ophthalmologic anomalies. Corneal opacification and shallow anterior chamber with synechiae are summarized as Peter’s anomaly. Other features may include congenital heart defects, hydrocephalus, seizures, and urogenital anomalies.