TY - CHAP M1 - Book, Section TI - Kocher-Debré-Sémélaigne Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is a congenital infantile disorder characterized by hypothyroidism with myxedema, muscular hypertrophy, short stature, macroglossia, cretinism, and mental retardation. The absence of painful spasms and pseudomyotonia differentiates this medical condition from the Hoffman Syndrome. It gives the infant a Hercules appearance! SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164075612 ER -