RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58088534
T1 Trisomy 9
T2 Syndromes: Rapid Recognition and Perioperative Implications
YR 2006
FD 2006
PB The McGraw-Hill Companies
PP New York, NY
SN 9780071354554
LK accessanesthesiology.mhmedical.com/content.aspx?aid=58088534
RD 2024/04/24
AB Chromosomal  disorder  that  can  occur  in  a  mosaic  or  nonmosaic  expression,  in  which  all  major  systems  are  significantly  involved.  Clinically  characterized  by  severe  gastrointestinal  problems,  scoliosis  and  kyphosis,  repetitive  periods  of  apnea,  complex  congenital  heart  defects,  severe  immunological  disorders,  failure  to  thrive,  and  severe  mental  retardation.  Death  occurs  in  infancy  or  early  childhood.