TY - CHAP M1 - Book, Section TI - Krause-van Schooneveld-Kivlin Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/10 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164075894 ER -