TY - CHAP M1 - Book, Section TI - Malpuech Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is a genetic disorder characterized by an association of mental retardation, dwarfism, hypertelorism, facial clefting (lip and palate), and caudal appendage. Other features include urogenital abnormalities (micropenis, hypospadias, renal anomalies), malar hypoplasia, large fontanelle, omphalocele, seizures, polycystic kidneys, and deafness. Cardiac and renal abnormalities may also be present. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164077652 ER -