RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164080727
T1 Orotic Aciduria
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=1164080727
RD 2024/04/24
AB Very  rare  congenital  disorder  characterized  by  an  inborn  error  of  pyrimidine  metabolism  resulting  in  hematologic  (megaloblastic  anemia  unresponsive  to  vitamin  C,  vitamin  B12,  or  folic  acid)  and  neurologic  (growth  and  mental  retardation)  manifestations.  Onset  in  childhood.