TY - CHAP M1 - Book, Section TI - Ullrich-Feichtiger Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164087118 ER -