TY  - CHAP
M1  - Book, Section
TI  - Schilder Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
Y1  - 2019
N1  - 
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - A  rare,  progressive,  and  lethal  disease  of  the  central  nervous  system  that  affects  mostly  children  and  characterized  by  adrenal  atrophy  and  diffuse  central  demyelination.  Presents  with  progressive  dementia,  spasticity,  cortical  blindness,  deafness,  hemiplegia,  quadriplegia,  ataxia,  pyramidal  signs,  retrobulbar  neuritis,  and  pseudobulbar  palsy.  Seizures.  Onset  in  late  childhood.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/19
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164084446
ER  -