RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164080362
T1 Noonan 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=1164080362
RD 2023/03/29
AB Part  of  group  of  RASopathies  (mutations  in  the  Ras/MAPK  pathway)  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.