RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58082352
T1 Otopalatodigital (OPD) Syndrome Type II
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=58082352
RD 2024/04/19
AB Genetic  disorder  involving  the  craniofacial,  oral,  and  osseous  structures,  characterized  by  short  stature,  unusual  facies,  cleft  palate,  and  multiple  skeletal  malformations.  Usually  psychomotor  development  is  normal,  but  some  affected  individuals  are  mentally  retarded.  Affected  males  show  a  very  high  incidence  of  neonatal  and  infancy  death.