Related Experiment Video
Updated: Jun 19, 2026

12:23
Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
AEC syndrome caused by a novel p63 mutation and demonstrating erythroderma followed by extensive depigmentation
David R Berk1, Kimberly Crone, Susan J Bayliss
1Division of Dermatology, Department of Internal Medicine, Washington University School of Medicine and St. Louis Children's Hospital, St. Louis, Missouri 63110, USA. dberk@im.wustl.edu
Pediatric Dermatology
|October 21, 2009
Abstract:
We present an infant with AEC syndrome due to a novel TP63 mutation (F552S), who demonstrated neonatal erythroderma followed by extensive depigmentation. We are unaware of previous reports highlighting the extensive depigmentation present in our patient.
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