TY - CHAP M1 - Book, Section TI - Michels Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is clinically defined as a triad of symptoms that include blepharophimosis, craniosynostosis, and epicanthus inversus. Other features include highly arched eyebrows, and hypertelorism. Occasional presence of spinal bifida occulta, cranial asymmetry, occipital bone flattening, and cleft lip/palate. Patient may manifest psychological development delays. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/11/11 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164078651 ER -