TY - CHAP M1 - Book, Section TI - Wadia-Swami Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164087736 ER -