RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164078812
T1 Miller 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=1164078812
RD 2024/04/17
AB It  is  a  congenital  disorder  characterized  by  postaxial  acrofacial  dysostosis  in  association  with  severe  postaxial  limb  deficiencies.  The  craniofacial  malformations  may  include  malar  hypoplasia,  micrognathia,  cleft  palate,  small,  protruding,  “cup-shaped”  ears,  eye  colobomas  and  ptosis,  and  ectropion.  The  limb  abnormalities  include  incomplete  hypoplasia,  syndactyly,  clinodactyly  (eg,  the  fifth  digits  and,  in  some  cases,  the  fourth  and  third  digits),  and  hypoplasia  of  the  ulna  and  occasionally  the  radius.