AEC Syndrome Caused by a Novel p63 Mutation and Demonstrating Erythroderma Followed by Extensive Depigmentation |
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| Authors: | DAVID R. BERK M.D. KIMBERLY CRONE M.D. SUSAN J. BAYLISS M.D. |
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| Affiliation: | Division of Dermatology, Departments of Internal Medicine and Pediatrics, Washington University School of Medicine and St. Louis Children's Hospital, St. Louis, Missouri |
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| Abstract: | 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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