RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58070389
T1 Familial Benign Copper Deficiency
T2 Syndromes: Rapid Recognition and Perioperative Implications
YR 2006
FD 2006
PB The McGraw-Hill Companies
PP New York, NY
SN 9780071354554
LK accessanesthesiology.mhmedical.com/content.aspx?aid=58070389
RD 2024/04/18
AB Infant  presenting  with  seizures  as  a  result  of  low  serum  copper  with  normal  ceruloplasmin  levels  and  normal  copper  urinary  excretion.  Improvement  of  the  physical  status  can  be  observed  following  oral  supplementation.  Postulated  to  result  from  a  defect  in  copper  absorption.