TY - CHAP M1 - Book, Section TI - Otopalatodigital (OPD) Syndrome Type I A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Marciniak, Bruno A1 - Dalens, Bernard J. PY - 2006 T2 - Syndromes: Rapid Recognition and Perioperative Implications AB - Rare congenital association characterized by hypertelorism, prominent supraorbital ridges, abnormal pinnae, broad nasal bridge with small nose and mouth, and downward-slanting palpebral fissures. Brachydactyly with cone-shaped epiphyses, cutaneous syndactyly, flattened tip of thumbs, splayed “frog” feet with a short hallux and a large gap between the first and second toes, and lateral curvature of the toes (clinodactyly on the fifth fingers and broad big toes). Other features include coarse facies, posterior cleft palate, and conduction deafness. The skull and limb are most often abnormal. SN - PB - The McGraw-Hill Companies CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=58082332 ER -