RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164074520
T1 Juvenile Paralysis Agitans of Hunt
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164074520
RD 2024/04/24
AB The  association  of  progressive  extrapyramidal  neurologic  disorder  presenting  in  teenagers  or  even  earlier  and  mild  form  of  Parkinson  disease.  Characterized  by  tremor,  bradykinesia,  dysarthria,  rigidity,  and  fixed  facies.  The  disorder  may  be  familial  (genetically  transmitted)  or  secondary  to  other  heredodegenerative  disorders,  as  it  is  observed  in  Huntington’s  disease.