AEC syndrome caused by a novel p63 mutation and demonstrating erythroderma followed by extensive depigmentation

David R. Berk; Kimberly Crone; Susan J. Bayliss

doi:10.1111/j.1525-1470.2009.00997.x

AEC syndrome caused by a novel p63 mutation and demonstrating erythroderma followed by extensive depigmentation

David R. Berk
, Kimberly Crone
, Susan J. Bayliss

Division of Dermatology

Research output: Contribution to journal › Article › peer-review

8 Scopus citations

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.

Original language	English
Pages (from-to)	617-618
Number of pages	2
Journal	Pediatric Dermatology
Volume	26
Issue number	5
DOIs	https://doi.org/10.1111/j.1525-1470.2009.00997.x
State	Published - Sep 2009

Access to Document

10.1111/j.1525-1470.2009.00997.x

Cite this

@article{85f4dbccfe7c41e78990fff0dbd4c487,

title = "AEC syndrome caused by a novel p63 mutation and demonstrating erythroderma followed by extensive depigmentation",

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.",

author = "Berk, \{David R.\} and Kimberly Crone and Bayliss, \{Susan J.\}",

year = "2009",

month = sep,

doi = "10.1111/j.1525-1470.2009.00997.x",

language = "English",

volume = "26",

pages = "617--618",

journal = "Pediatric Dermatology",

issn = "0736-8046",

number = "5",

}

TY - JOUR

T1 - AEC syndrome caused by a novel p63 mutation and demonstrating erythroderma followed by extensive depigmentation

AU - Berk, David R.

AU - Crone, Kimberly

AU - Bayliss, Susan J.

PY - 2009/9

Y1 - 2009/9

N2 - 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.

AB - 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.

UR - https://www.scopus.com/pages/publications/70350006694

U2 - 10.1111/j.1525-1470.2009.00997.x

DO - 10.1111/j.1525-1470.2009.00997.x

M3 - Article

C2 - 19840326

AN - SCOPUS:70350006694

SN - 0736-8046

VL - 26

SP - 617

EP - 618

JO - Pediatric Dermatology

JF - Pediatric Dermatology

IS - 5

ER -

AEC syndrome caused by a novel p63 mutation and demonstrating erythroderma followed by extensive depigmentation

Abstract

Access to Document

Other files and links

Fingerprint

Cite this