TY  - CHAP
M1  - Book, Section
TI  - Machado-Joseph Disease
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
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.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58075013
ER  -