TY  - CHAP
M1  - Book, Section
TI  - Hyperprolinemia
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - Inborn  error  of  metabolism  resulting  from  a  defect  in  renal  tubular  amino  acid  transport  leading  to  abnormal  urinary  excretion  of  glycine,  proline,  and  hydroxyproline.  The  clinical  features  of  this  medical  condition  are  seizures  and  variable  intellectual  disabilities.  The  presence  of  lactic  academia,  particularly  in  Type  II  Hyperprolinemia  must  be  considered.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/18
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164073383
ER  -