TY  - CHAP
M1  - Book, Section
TI  - Otopalatodigital (OPD) Syndrome Type II
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
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.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/18
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58082352
ER  -