Source:http://linkedlifedata.com/resource/pubmed/id/19005244
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2009-1-30
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pubmed:abstractText |
Epidermodysplasia verruciformis (EV) is a rare autosomal-recessive disorder characterized by widespread and persistent infection with human papilloma virus (HPV) and a risk of malignant degeneration. Most cases of EV are caused by mutations in the two EV genes, EVER1/TMC6 and EVER2/TMC8. The clinical presentation of EV takes two different forms, which coexist in most cases. Over a period of years, patients develop plane warts and pityriasis versicolor-like lesions. Sixteen cases of EV in HIV-positive patients have been clinically investigated and reported in the literature. However, different inherited susceptibilities towards HPV infection in immunodeficient patients, like HIV-positive patients, have only rarely been addressed.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
1421-9832
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pubmed:author | |
pubmed:copyrightInfo |
Copyright (c) 2008 S. Karger AG, Basel.
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pubmed:issnType |
Electronic
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pubmed:volume |
218
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
114-8
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pubmed:meshHeading |
pubmed-meshheading:19005244-AIDS-Related Opportunistic Infections,
pubmed-meshheading:19005244-Adult,
pubmed-meshheading:19005244-Alanine,
pubmed-meshheading:19005244-Epidermodysplasia Verruciformis,
pubmed-meshheading:19005244-Female,
pubmed-meshheading:19005244-HIV Infections,
pubmed-meshheading:19005244-Homozygote,
pubmed-meshheading:19005244-Humans,
pubmed-meshheading:19005244-Immunocompromised Host,
pubmed-meshheading:19005244-Membrane Proteins,
pubmed-meshheading:19005244-Mutation,
pubmed-meshheading:19005244-Papillomaviridae,
pubmed-meshheading:19005244-Polymorphism, Single Nucleotide,
pubmed-meshheading:19005244-Threonine
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pubmed:year |
2009
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pubmed:articleTitle |
Epidermodysplasia verruciformis in a HIV-positive patient homozygous for the c917A-->T polymorphism in the TMC8/EVER2 gene.
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pubmed:affiliation |
Department of Dermatology, Kantonsspital Aarau, Aarau, Switzerland.
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pubmed:publicationType |
Journal Article,
Case Reports
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