RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58081794
T1 Noonan Syndrome
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=58081794
RD 2024/04/20
AB Rare  genetic  disorder  present  at  birth.  Characterized  by  distinctive  facial  appearance,  broad  or  webbed  neck,  low  hairline  in  the  back  of  the  head,  and  short  stature.  Micrognathia,  kyphosis  and/or  scoliosis,  and  cardiac  defects  (pulmonary  valvular  stenosis)  are  present.  Other  features  include  coagulation  disorders,  platelet  deficiencies,  mild  mental  retardation,  and  cryptorchidism  in  the  first  year  of  life.