Kindler syndrome: report of two cases and review of the literature.

Abstract:

:We evaluated two patients with hereditary bullous poikiloderma. Both had acral bullae, generalized poikiloderma with prominent atrophy, and acral keratoses. One patient, with sporadic disease, had, in addition, urethral and subglottic stenoses, webbing of digits, and poor dentition. The other patient, whose disease was dominantly inherited, had koilonychia. The results of cutaneous histopathology, electron microscopy, and immunofluorescence mapping studies are presented. It is possible that Kindler syndrome and Weary's hereditary acrokeratotic poikiloderma are variants of the same disease.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Forman AB,Prendiville JS,Esterly NB,Hebert AA,Duvic M,Horiguchi Y,Fine JD

doi

10.1111/j.1525-1470.1989.tb01004.x

subject

Has Abstract

pub_date

1989-06-01 00:00:00

pages

91-101

issue

2

eissn

0736-8046

issn

1525-1470

journal_volume

6

pub_type

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