RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164075949
T1 Krieble-Bixler Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accesspediatrics.mhmedical.com/content.aspx?aid=1164075949
RD 2024/04/18
AB It  is  an  inherited  medical  condition  characterized  by  craniofacial  area  and  skeletal  abnormalities.  The  clinical  features  include  craniosynostosis,  prominent  forehead,  midface  hypoplasia,  proptosis  and  ocular  hypotelorism,  submucosal  cleft  palate,  radiohumeral  or  radioulnar  dysostosis,  arachnodactyly,  particularly  a  clinodactyly  of  the  fifth  finger,  and  hypospadias.  It  may  present  with  tetralogy  of  Fallot  and  short  stature  (dwarfism).