TY  - CHAP
M1  - Book, Section
TI  - Hunter 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  disorder  characterized  by  the  accumulation  of  acid  mucopolysaccharides  (heparan  and  dermatan  sulfates)  in  the  central  nervous  system  and  peripheral  tissues,  affecting  only  male  children  and  resulting  in  severe  neurologic  impairment.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/16
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164073191
ER  -