RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164073888 T1 Infantile-Onset Spinocerebellar Ataxia (IOSCA) 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=1164073888 RD 2024/03/28 AB ☞Spinocerebellar Syndrome, also known as spinocerebellar atrophy or spinocerebellar degeneration, is a progressive, degenerative with multiple types, with an estimated 150,000 people in the United States. Spinocerebellar ataxia (SCA) is hereditary, progressive, and often fatal. There is no known effective treatment or cure. SCA can affect anyone of any age.