TY - CHAP M1 - Book, Section TI - Machado-Joseph Disease A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164077525 ER -