TY  - CHAP
M1  - Book, Section
TI  - Ramsay Hunt Syndrome Type I
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - A  very  rare  genetic  disorder  characterized  by  predominant  neurological  syndrome  (myoclonus,  occasional  tonic-chronic  seizures,  and  ataxia)  with  alteration  of  cerebellum  and  globus  pallidus.  Muscular  functions  can  also  be  affected.  No  underlying  mitochondrial  myopathy.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/18
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=1164083239
ER  -