RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58089463
T1 Waardenburg Syndrome
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=58089463
RD 2024/04/19
AB An  auditory  pigmentary  syndrome  characterized  by  hypopigmentation  of  the  skin,  iris,  hair  and  stria  vascularis  of  the  cochlea.  Most  patients  present  with  two  different  colored  eyes,  white  forelock  and  eyelashes,  and  premature  graying  of  the  hair.  Moderate  acrocephaly,  lack  of  osseous  fusion  of  the  short  tubular  bones,  oligodactyly  of  the  feet,  short  stature,  pericardial  cysts,  rectal  prolapse,  and  deformed  ears  are  reported.  Other  features  include  hypoplastic  maxilla,  asymmetry  of  hands,  deformity  of  the  first  phalanx  of  the  head,  absence  of  the  first  digit  of  the  foot,  and  bifid  distal  phalanges  of  the  second  and  third  toes.