RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164076653 T1 Lenz-Majewski Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164076653 RD 2024/03/28 AB It is characterized by multiple congenital anomalies (delayed closure of fontanel, proximal symphalangism, prominent scalp cutaneous veins), mental retardation, and progressive skeletal osteosclerosis with severe growth retardation and a progeroid appearance. Other clinical features include dysplastic teeth, skin hypoplasia joint laxity, choanal atresia, short digits, and partial syndactyly.