RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164087736 T1 Wadia-Swami Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164087736 RD 2024/10/08 AB This is a medical disorder part of a larger group of spinocerebellar degeneration syndromes. Clinically, it is characterized by abnormal eye movements described as absent rapid saccades (scanning) and abnormally slow pursuit (tracking). Individual affected with this syndrome usually die within 10 years of the onset of symptoms. Autosomal dominant cerebellar ataxias are a heterogeneous group of disorders. Progressive cerebellar ataxia is the primary feature. The infantile onset is characterized by neonatal hypotonia, developmental delay, and severe dysphagia.