RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164080849
T1 Otopalatodigital (OPD) Syndrome Type I
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=1164080849
RD 2024/04/19
AB Rare  congenital  association  characterized  by  coarse  facial  features  (hypertelorism,  prominent  supraorbital  ridges,  abnormal  pinnae,  broad  nasal  bridge  with  small  nose  and  mouth,  and  downward-slanting  palpebral  fissures),  posterior  cleft  palate,  conduction  deafness,  and  broad  distal  digits  with  short  nails.