TY  - CHAP
M1  - Book, Section
TI  - Hallervorden-Spatz Disease
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - Inherited  disorder  characterized  by  progressive  degeneration  of  the  nervous  system  caused  by  iron  deposition  in  basal  ganglia.  Most  commonly  begins  in  childhood  as  a  dystonic  syndrome.  Other  clinical  features  include  distorting  muscle  contractions  of  the  face,  limbs,  and  trunk,  choreoathetosis,  muscle  rigidity,  spasticity,  seizures,  and  dementia.  Less  common  symptoms  include  painful  muscle  spasms,  mental  retardation,  and  visual  impairment.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/25
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=1164072014
ER  -