RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164061035
T1 Aicardi-Goutières Syndrome (AGS)
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=1164061035
RD 2024/10/03
AB A  rapidly  progressive,  familial  encephalopathy  with  calcifications  of  the  basal  ganglia,  cerebral  white  matter  abnormalities,  cerebral  atrophy,  progressive  microcephaly,  chronic  cerebrospinal  fluid  (CSF)  lymphocytosis,  and  elevated  levels  of  interferon-α  in  CSF  and  serum.  This  syndrome  may  progress  fast  into  a  vegetative  state  and  early  death.