TY - CHAP M1 - Book, Section TI - Ectrodactyly, Ectodermal Dysplasia, and Clefting (EEC) Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/15 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164068735 ER -