TY - CHAP M1 - Book, Section TI - Marden-Walker Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is a very rare inherited connective tissue disorder that is characterized by in 75% of affected children, blepharophimosis, a small mouth, micrognathia, kyphoscoliosis, radioulnar synostosis, and multiple joint contractures. Other clinical features include microcytic dysplastic kidneys, dextrocardia, Dandy-Walker malformation, agenesis of the corpus callosum, arachnodactyly, camptodactyly, cleft lip/palate or a high-arched palate, growth delay, and slow muscle movement. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164077737 ER -