RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164087118 T1 Ullrich-Feichtiger Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164087118 RD 2024/03/29 AB A congenital syndrome characterized by an association of micrognathia, ocular, dental, and genital malformations. Other features include deafness, rudimentary toes, clubfoot, partial atresia of the anus, hypospadias, and mask-like facies. A number of authors have suggested that this syndrome is a variant of Smith-Lemli-Opitz Syndrome.