RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164082467
T1 Prolidase Deficiency
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=1164082467
RD 2024/04/16
AB A  rare  congenital  disorder  of  the  small  peptides  metabolism  (imidazoles  dipeptides).  It  is  characterized  by  mild  to  severe  skin  lesions  (mostly  the  face,  palms,  lower  legs,  and  soles),  cognitive  impairment,  splenomegaly,  recurrent  infections  involving  mainly  the  respiratory  system,  and  iminodipeptiduria.