RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164078082
T1 McPherson-Clemens 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=1164078082
RD 2024/04/23
AB It  is  a  very  rare,  autosomal  recessive  disorder  characterized  by  bilateral  cleft  lip  and  palate,  hypertelorism,  flat  facial  profile,  bifid  thumbs,  flat  occiput,  complex  congenital  heart  defect,  and  malrotation  of  the  intestine.