TY  - CHAP
M1  - Book, Section
TI  - Opitz-Frias Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
Y1  - 2006
N1  - 
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - Genetic  disorder  characterized  by  craniofacial  anomalies,  ocular  hypertelorism,  cleft  lip  and  palate,  epicanthal  folds,  and  a  wide,  flat  nasal  bridge.  Affected  males  present  cryptorchidism,  bifid  scrotum,  and/or  hypospadias.  The  most  significant  anomalies  are  the  presence  of  cleft  in  the  larynx  and  trachea,  pulmonary  hypoplasia,  dysphagia,  and  respiratory  obstruction.  Hypoplasia  or  agenesis  of  the  corpus  callosum,  kidney  abnormalities,  cardiac  defects,  and  mental  retardation  have  been  reported.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58082095
ER  -