Medizinische Universität Graz - Research portal
Selected Publication:
Binder, B; Metze, D; Smolle, J.
Congenital bullous poikiloderma (Kindler syndrome)
Hautarzt. 2002; 53(8):546-549
Doi: 10.1007/s00105-001-0327-3
(- Case Report)
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- Leading authors Med Uni Graz
- Binder Barbara
- Co-authors Med Uni Graz
- Smolle Josef
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- 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 poikoloderma 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.
- Find related publications in this database (using NLM MeSH Indexing)
- Adolescent -
- Basement Membrane - pathology
- Chromosome Aberrations - pathology
- Female - pathology
- Genes, Recessive - pathology
- Humans - pathology
- Microscopy, Electron - pathology
- Rothmund-Thomson Syndrome - diagnosis
- Skin - pathology
- Find related publications in this database (Keywords)
- congenital blisters
- poikiloderma
- Kindler syndrome