RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164077525 T1 Machado-Joseph Disease 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=1164077525 RD 2024/10/06 AB It is a rare hereditary neurodegenerative disorder, also called Spinocerebellar Ataxia Type III, which is characterized by weakness of arms and legs, spasticity, and a staggering lurching gait easily mistaken from drunkenness. Other clinical features include dysphagia, severe nystagmus, dystonia, and twitching of the tongue. Some patients have peculiar exophthalmos.