RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164075558
T1 Knobloch 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=1164075558
RD 2024/04/20
AB An  inherited  disorder  characterized  by  encephalocele,  vitreoretinal  degeneration  with  retinal  detachment,  high  myopia,  and  normal  intelligence.  It  is  also  characterized  by  cataracts,  and  the  association  with  skull  defects  such  as  occipital  encephalocele  and  occipital  aplasia.  Meningocele  have  also  been  reported  as  part  of  this  medical  disorder.