RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164065476
T1 CHILD Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accesspediatrics.mhmedical.com/content.aspx?aid=1164065476
RD 2024/04/20
AB An  inherited  syndrome  characterized  by  a  unilateral  ichthyosiform  erythroderma  with  strict  midline  demarcation  sparing  the  face  and  ipsilateral  defects  involving  all  skeletal  structures  and  internal  organs.  CHILD  is  an  acronym  that  stands  for  Congenital  Hemidysplasia  with  Ichthyosiform  erythroderma,  and  Limb  Defects.