TY  - CHAP
M1  - Book, Section
TI  - Noonan Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
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.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/18
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=1164080362
ER  -