RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164061008
T1 Aicardi Syndrome
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=1164061008
RD 2024/04/25
AB A  disorder  that  affects  only  females  and  is  characterized  by  the  triad  of  partial  or  complete  agenesis  of  the  corpus  callosum,  infantile  spasms  (spasm-like  epilepsy),  and  distinctive  chorioretinal  lacunae.  This  syndrome  often  associated  with  other  features,  such  as  mental  retardation,  microcephaly,  and  porencephalic  cysts.  Onset  is  generally  between  3  and  5  months  of  age.