RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58076462
T1 Molybdenum Cofactor 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=58076462
RD 2024/09/12
AB Extremely  rare,  congenital,  severe  neurologic  anomalies  including  seizures,  spastic  tetraparesis,  brain  atrophy,  mental  retardation,  abnormal  muscle  tone  and  myoclonic  spasms,  dislocated  lenses,  and  xanthine  urinary  stones.