TY - CHAP M1 - Book, Section TI - Otopalatodigital (OPD) Syndrome Type I A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Rare congenital association characterized by coarse facial features (hypertelorism, prominent supraorbital ridges, abnormal pinnae, broad nasal bridge with small nose and mouth, and downward-slanting palpebral fissures), posterior cleft palate, conduction deafness, and broad distal digits with short nails. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164080849 ER -