Ulerythema ophryogenes in Cornelia de Lange syndrome.

Abstract:

:A 17-year-old woman with Cornelia de Lange syndrome had asymptomatic skin lesions since the age of 4 years. These were multiple, follicular, horny papules, present on both cheeks, and surrounded by erythematous skin. Similar lesions were present on the external aspect of the arms, but amidst skin of normal coloration. Keratosis pilaris atrophicans faciei (ulerythema ophryogenes) has been described as a cutaneous marker for several congenital syndromes. To our knowledge, its possible association with Cornelia de Lange syndrome has never been reported.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Flórez A,Fernández-Redondo V,Toribio J

doi

10.1046/j.1525-1470.2002.00003.x

subject

Has Abstract

pub_date

2002-01-01 00:00:00

pages

42-5

issue

1

eissn

0736-8046

issn

1525-1470

pii

0003

journal_volume

19

pub_type

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