RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164068735 T1 Ectrodactyly, Ectodermal Dysplasia, and Clefting (EEC) 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=1164068735 RD 2024/10/15 AB Autosomal dominant inherited syndrome characterized by the triad of ectrodactyly, ectodermal dysplasia, and facial clefts (lip and palate). Other clinical features include maxillary hypoplasia, mild malar hypoplasia, choanal atresia, conductive hearing loss, photophobia and blepharophimosis, dacryocystitis, cryptorchidism, hypogonadotropic hypogonadism renal agenesis or dysplasia, hydronephrosis, occasionally mental retardation, central diabetes insipidus.