TY - CHAP M1 - Book, Section TI - Infantile-Onset Spinocerebellar Ataxia (IOSCA) A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164073888 ER -