RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164068857
T1 Ellis-van Creveld 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=1164068857
RD 2023/06/05
AB It  is  a  rare  genetic  disorder  characterized  by  short  limb  dwarfism,  polydactyly  of  the  hands  and  feet,  abnormal  development  of  fingernails  and,  in  more  than  50%  congenital  heart  defects.  The  most  common  heart  defect  include  atrial  septal  defect,  ventricular  septal  defect,  and  patent  ductus  arteriosus.  Urogenital  anomalies  have  also  been  reported  in  males  only,  particularly  cryptorchidism  and  epispadias,  but  are  not  considered  characteristics  of  this  medical  condition.  Motor  development  and  intelligence  are  normal.