RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Marciniak, Bruno A1 Dalens, Bernard J. SR Print(0) ID 58061093 T1 Ablepharon-Macrostomia Syndrome (AMS) T2 Syndromes: Rapid Recognition and Perioperative Implications YR 2006 FD 2006 PB The McGraw-Hill Companies PP New York, NY SN 9780071354554 LK accessanesthesiology.mhmedical.com/content.aspx?aid=58061093 RD 2024/11/01 AB Quantitative and qualitative defects in development of the prosencephalic neural crest. Fish-like facial (mouth) appearance. Other craniofacial anomalies include triangularly shaped face, small nose, partial absence of tissue (coloboma) from the midportion of nostril walls. Heart, kidney, and liver anomalies are present, especially in neonates. Other features include skin and genitalia anomalies, absent eyelids, alopecia totalis, camptodactyly. Infants and children with AMS show delayed language development and mental retardation.