TY - CHAP M1 - Book, Section TI - CHILD Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - An inherited syndrome characterized by a unilateral ichthyosiform erythroderma with strict midline demarcation sparing the face and ipsilateral defects involving all skeletal structures and internal organs. CHILD is an acronym that stands for Congenital Hemidysplasia with Ichthyosiform erythroderma, and Limb Defects. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164065476 ER -