RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164075612
T1 Kocher-Debré-Sémélaigne 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=1164075612
RD 2024/04/23
AB It  is  a  congenital  infantile  disorder  characterized  by  hypothyroidism  with  myxedema,  muscular  hypertrophy,  short  stature,  macroglossia,  cretinism,  and  mental  retardation.  The  absence  of  painful  spasms  and  pseudomyotonia  differentiates  this  medical  condition  from  the  Hoffman  Syndrome.  It  gives  the  infant  a  Hercules  appearance!