RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164070963
T1 Glycogen Storage Diseases (GSD): An Overview
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164070963
RD 2024/04/18
AB There  are  fifteen  distinct  glycogen  storage  diseases.  Although  glycogen  synthase  deficiency  does  not  result  in  storage  of  extra  glycogen  in  the  liver,  it  is  usually  classified  with  the  GSD  Type  0  because  it  is  another  defect  of  glycogen  storage  and  can  cause  similar  problems.  The  overall  frequency  of  glycogen-storage  disease  has  been  established  approximately  1:20,000  to  25,000  people  worldwide.