RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164077737 T1 Marden-Walker 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=1164077737 RD 2023/02/02 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.