RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164086845
T1 Trisomy 9
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=1164086845
RD 2024/04/19
AB Chromosomal  disorder  that  can  occur  in  a  mosaic  or  nonmosaic  expression,  in  which  all  major  systems  are  significantly  involved.  Clinically  characterized  by  failure  to  thrive,  severe  intellectual  disability,  skeletal  abnormalities  (kyphoscoliosis,  joint  anomalies),  severe  gastroesophageal  reflux,  craniofacial  malformations,  complex  congenital  heart  defects.  Death  occurs  mostly  in  infancy  or  early  childhood.