RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58075013
T1 Machado-Joseph Disease
T2 Syndromes: Rapid Recognition and Perioperative Implications
YR 2006
FD 2006
PB The McGraw-Hill Companies
PP New York, NY
SN 9780071354554
LK accessanesthesiology.mhmedical.com/content.aspx?aid=58075013
RD 2022/08/11
AB 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.