RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164069415 T1 Familial Benign Copper Deficiency T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164069415 RD 2024/03/28 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.