TY - CHAP M1 - Book, Section TI - Mowat-Wilson Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is an autosomal dominant complex developmental disorder characterized by the association of Hirschsprung’s disease, intellectual disability, and epilepsy. Other features include short stature, microcephaly, severe mental retardation, delayed motor development, epilepsy, and a wide spectrum of clinically heterogeneous features suggestive of neurocristopathies at the cephalic, cardiac, and vagal nerve levels. The presence of congenital heart disease, genitourinary anomalies and absence of the corpus callosum complete the diagnosis. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164079297 ER -