TY  - CHAP
M1  - Book, Section
TI  - Melnick-Fraser Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - Very  rare  genetic  disorder  characterized  by  distinctive  malformations  of  the  head  and  facial  area,  with  skin  lesions  and  abnormalities  of  the  eyes.  Other  clinical  features  may  include  renal  anomalies  (bilateral  renal  dysplasia),  Mendini-type  cochlear  malformation  (hypoplasia  of  cochlear  apex  on  CT  scan),  bilateral  prehelical  pits,  and  bilateral  branchial  cleft  fistulas.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58075748
ER  -