TY - CHAP M1 - Book, Section TI - Muller Barth Menger Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is a genetic disease characterized by the presence of multiple cerebral malformation, seizures, hypertrichosis, distinct face, claw hands, and overlapping fingers. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164079502 ER -