RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164076545
T1 Leiner 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=1164076545
RD 2024/04/19
AB It  is  a  severe  skin  disorder  characterized  by  erythroderma  with  an  onset  during  infancy.  The  presence  of  seborrheic  dermatitis,  diarrhea,  and  recurrent  systemic  infections  defines  this  medical  condition.  Other  features  include  large  patches  of  red  skin,  and  delayed  central  nervous  system  development  due  to  complement  C5  deficiency  (acquired  deficiency  in  most  patients).