TY - CHAP M1 - Book, Section TI - Keratitis Ichthyosis Deafness (KID) Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is a rare disease associated with ectodermal dysplasia characterized by inflammation of the corneae (keratitis), erythrokeratoderma, skin scaling (ichthyosis) especially the palms of the hands and sole of the feet, and sensorineural deafness. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164075094 ER -