RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58082332
T1 Otopalatodigital (OPD) Syndrome Type I
T2 Syndromes: Rapid Recognition and Perioperative Implications
YR 2006
FD 2006
PB The McGraw-Hill Companies
PP New York, NY
SN 9780071354554
LK accessanesthesiology.mhmedical.com/content.aspx?aid=58082332
RD 2024/04/19
AB Rare  congenital  association  characterized  by  hypertelorism,  prominent  supraorbital  ridges,  abnormal  pinnae,  broad  nasal  bridge  with  small  nose  and  mouth,  and  downward-slanting  palpebral  fissures.  Brachydactyly  with  cone-shaped  epiphyses,  cutaneous  syndactyly,  flattened  tip  of  thumbs,  splayed  “frog”  feet  with  a  short  hallux  and  a  large  gap  between  the  first  and  second  toes,  and  lateral  curvature  of  the  toes  (clinodactyly  on  the  fifth  fingers  and  broad  big  toes).  Other  features  include  coarse  facies,  posterior  cleft  palate,  and  conduction  deafness.  The  skull  and  limb  are  most  often  abnormal.