RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164082133 T1 Porokeratosis of Mibelli T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164082133 RD 2024/03/28 AB Congenital or acquired genodermatosis disorder of keratinization. Clinically, presents one or more atrophic patches surrounded by a distinctive ridge-like border called the cornoid lamella. Several variants are described with the disseminated superficial actinic porokeratosis being relatively common.