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Congenital bullous poikiloderma (Kindler syndrome)
Author(s): Binder B, Metze D, Smolle J
Source: HAUTARZT    Volume: 53    Issue: 8    Pages: 546-549    Published: AUG 2002  
Times Cited: 5     References: 9     
Abstract: We report on an 18 years old female patient who presented with synechia of the labia. History reveals congenital blistering with acral localization and photosensitivity in childhood. At present, the patient showed wide-spread poilkoloderma with reticulate hyperpigmentation, xerosis, proximal synechia between fingers and toes and absence of dermatoglyphics, suggestive for congenital bullous poikiloderma (Kindler syndrome) The diagnosis was confirmed by histology and electron microscopy. Kindler syndrome is a rare, autosomal recessive disorder with synechia of mucosal areas being the presenting symptom.
Document Type: Article
Language: German
Reprint Address: Binder, B (reprint author), Graz Univ, Dermatol Klin, Auenbruggerpl 8, A-8036 Graz, Austria
Addresses:
1. Graz Univ, Dermatol & Venereol Klin, A-8036 Graz, Austria
2. Univ Munster, Haut Klin, D-4400 Munster, Germany
Publisher: SPRINGER-VERLAG, 175 FIFTH AVE, NEW YORK, NY 10010 USA
Subject Category: Dermatology
IDS Number: 584QR
ISSN: 0017-8470
DOI: 10.1007/s00105-001-0327-3
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