TY - CHAP M1 - Book, Section TI - McPherson-Clemens Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is a very rare, autosomal recessive disorder characterized by bilateral cleft lip and palate, hypertelorism, flat facial profile, bifid thumbs, flat occiput, complex congenital heart defect, and malrotation of the intestine. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164078082 ER -