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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2010-7-21
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pubmed:abstractText |
Galli-Galli disease (GGD) is a rare genodermatosis. Its clinical presentation is identical to that of Dowling-Degos disease (DDD), but the presence of the histopathological feature of acantholysis in GGD is thought to distinguish the two disorders. Mutations in the keratin 5 gene (KRT5) have been identified in the majority of patients with DDD and in a small number of patients with GGD.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1365-2133
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pubmed:author |
pubmed-author:BetzR CRC,
pubmed-author:Braun-FalcoMM,
pubmed-author:EigelshovenSS,
pubmed-author:El Shabrawi-CaelenLL,
pubmed-author:HannekenSS,
pubmed-author:LVOVAT NTN,
pubmed-author:NöthenM MMM,
pubmed-author:PasternackS MSM,
pubmed-author:RuzickaTT,
pubmed-author:WattelCC,
pubmed-author:WenzelJJ
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pubmed:issnType |
Electronic
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pubmed:volume |
163
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
197-200
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pubmed:meshHeading |
pubmed-meshheading:20222933-Acantholysis,
pubmed-meshheading:20222933-Adolescent,
pubmed-meshheading:20222933-Adult,
pubmed-meshheading:20222933-Diagnosis, Differential,
pubmed-meshheading:20222933-Female,
pubmed-meshheading:20222933-Genetic Predisposition to Disease,
pubmed-meshheading:20222933-Humans,
pubmed-meshheading:20222933-Hyperpigmentation,
pubmed-meshheading:20222933-Keratin-5,
pubmed-meshheading:20222933-Male,
pubmed-meshheading:20222933-Malignant Atrophic Papulosis,
pubmed-meshheading:20222933-Mutation,
pubmed-meshheading:20222933-Pedigree,
pubmed-meshheading:20222933-Young Adult
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pubmed:year |
2010
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pubmed:articleTitle |
Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease.
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pubmed:affiliation |
Department of Dermatology, University Hospital Düsseldorf, Moorenstrasse 5, 40225 Düsseldorf, Germany. Hanneken@med.uni-duesseldorf.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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