RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164077978
T1 Mauriac Syndrome
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=1164077978
RD 2024/04/16
AB It  is  a  very  rare  metabolic  disorder  characterized  by  early  onset  of  diabetes  mellitus  in  the  infancy  period,  cushingoid  features  (moon  face-like  appearance),  multiple  epiphyseal  dysplasia,  multiple  fractures,  microcephaly,  short  stature,  hypertonia,  barrel-shaped  chest,  hepatomegaly,  tooth  discoloration,  gray-blue  sclerae,  high-arched  palate,  and  skin  abnormalities.  Epiphyseal  dysplasia  and  growth  retardation  have  onset  within  the  first  2  years  of  life.