TY  - CHAP
M1  - Book, Section
TI  - Uridine Diphosphate Galactose Epimerase Deficiency
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - A  disorder  of  galactose  metabolism  characterized  by  a  deficiency  of  uridylyl  diphosphogalactose-4-epimerase  activity  resulting  in  benign  asymptomatic  form  (deficiency  in  blood  cells  only)  and  severe  forms  with  hepatic  failure,  Fanconi  syndrome,  and  neurological  impairment.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58088980
ER  -