RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164069127
T1 Eronen 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=1164069127
RD 2024/04/18
AB It  is  a  very  rare  disorder  inherited  as  an  autosomal  recessive  pattern  and  characterized  by  the  absence  or  severe  digital  phalanges  abnormalities  of  the  fingers  and  toes,  renal  defects,  and  cerebral  malformations,  particularly  ventricles  dilatation,  raised  intracranial  pressure,  and  prolonged  seizures.  Affected  individuals  present  profound  intellectual  disabilities.