TY - CHAP M1 - Book, Section TI - Stickler Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164085749 ER -