RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58061093
T1 Ablepharon-Macrostomia Syndrome (AMS)
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=58061093
RD 2024/04/24
AB Quantitative  and  qualitative  defects  in  development  of  the  prosencephalic  neural  crest.  Fish-like  facial  (mouth)  appearance.  Other  craniofacial  anomalies  include  triangularly  shaped  face,  small  nose,  partial  absence  of  tissue  (coloboma)  from  the  midportion  of  nostril  walls.  Heart,  kidney,  and  liver  anomalies  are  present,  especially  in  neonates.  Other  features  include  skin  and  genitalia  anomalies,  absent  eyelids,  alopecia  totalis,  camptodactyly.  Infants  and  children  with  AMS  show  delayed  language  development  and  mental  retardation.