RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58072933
T1 Knobloch Syndrome
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=58072933
RD 2024/04/23
AB An  inherited  disorder  characterized  by  encephalocele,  vitroretinal  degeneration  with  retinal  detachment,  high  myopia,  and  normal  intelligence.  Because  all  patients  have  normal  intelligence,  it  is  suggested  that  the  cephalocele  is  a  meningocele  rather  than  an  encephalocele.