TY  - CHAP
M1  - Book, Section
TI  - Stickler Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - Stickler  syndrome  is  an  autosomal  dominant  hereditary  progressive  arthro-ophthalmology  condition  characterized  by  congenital  abnormalities  of  the  eye,  micrognathia,  and  a  cleft  palate.  Other  clinical  features  include  flat  midface,  intracranial  calcifications,  and  deafness.  More  than  50%  of  patients  affected  with  this  condition  have  a  mitral  valve  prolapse  and  authors  have  suggested  that  in  the  presence  of  an  autosomal  dominant  inherited  mitral  valve  prolapse,  a  Stickler  syndrome  should  be  suspected  until  proven  otherwise.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/18
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58087358
ER  -