TY  - CHAP
M1  - Book, Section
TI  - Orotic Aciduria
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
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.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/18
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164080727
ER  -