RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164075913
T1 Krause-Reese Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accesspediatrics.mhmedical.com/content.aspx?aid=1164075913
RD 2024/04/19
AB It  is  an  inherited  syndrome  characterized  by  multiple  ocular  malformations  in  association  with  microcephaly.  It  is  more  commonly  found  in  premature  infants  and  in  single  infants  of  multiple  births.  It  is  characterized  by  the  presence  of  retinal  and  cerebral  dysplasia,  microphthalmos,  retinal  choroid  and  optic  nerve  malformations,  retinal  glial  membranes,  hyperplasia  or  aplasia  of  the  brain  and  cerebellum,  and  microcephaly.  Other  features  include  mental  retardation,  hydrocephalus,  blindness,  enophthalmos,  microphthalmos,  strabismus,  retinal  atrophy,  gliosis,  retinal  and  vitreous  hemorrhages,  synechiae,  glaucoma,  and  cataract.