RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164086915
T1 Trisomy 18
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=1164086915
RD 2024/04/23
AB Chromosomal  disorder  characterized  by  a  broad  spectrum  of  variable  dysmorphic  features  (hypoplastic  mandible  and  maxilla)  and  organ  malformations  (atrial  septal  defect  [ASD],  ventricular  septal  defect  [VSD],  omphalocele)  with  extremely  poor  prognosis  (90%  of  patients  die  before  1  year  of  age).