RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164073712
T1 Iminoglycinuria
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=1164073712
RD 2024/04/25
AB It  is  a  benign  inborn  error  of  metabolism  caused  by  a  defect  in  renal  tubular  amino  acid  transport  resulting  in  abnormal  urinary  excretion  of  glycine,  proline,  and  hydroxyproline.  The  clinical  manifestations  include  encephalopathy,  mental  retardation,  deafness,  blindness,  renal  lithiasis,  mild  to  severe  hypertension,  and  cerebral  (gyrate)  atrophy.