TY  - CHAP
M1  - Book, Section
TI  - Hurler Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - Genetically  transmitted  lysosomal  storage  disease  resulting  in  accumulation  of  acid  mucopolysaccharides  in  the  central  nervous  system  and  peripheral  tissues  characterized  by  coarse  facies  (gargoyle-like),  profound  mental  retardation,  considerable  hepatomegaly,  hernias,  enlarged  tongue,  skeletal  disorders  (kyphoscoliosis),  dwarfism,  and  respiratory  and  cardiac  impairment.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/16
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=1164073246
ER  -