RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164085749 T1 Stickler Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164085749 RD 2024/03/29 AB Stickler Syndrome is a hereditary progressive ophthalmo-arthropathy 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.