TY  - CHAP
M1  - Book, Section
TI  - Otopalatodigital (OPD) Syndrome Type II
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - Genetic  disorder  involving  the  craniofacial,  oral,  and  osseous  structures,  characterized  by  short  stature,  unusual  facies,  cleft  palate,  and  multiple  skeletal  malformations.  More  severe  form.  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  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/18
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164080875
ER  -