RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164079110
T1 Molybdenum Cofactor Deficiency
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=1164079110
RD 2024/04/20
AB It  is  an  extremely  rare  severe  progressive  neurodegenerative  and  neurometabolic  disease,  characterized  by  convulsions,  severe  mental  and  motor  retardation  resistant  to  the  treatment.  Other  features  include  spastic  tetraparesis,  brain  atrophy,  abnormal  muscle  tone,  myoclonic  spasms,  dislocated  lenses,  and  xanthine  urinary  stones.