Source:http://linkedlifedata.com/resource/pubmed/id/20618471
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2010-7-12
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pubmed:abstractText |
Olmsted syndrome is a rare keratinization disorder characterized by mutilating palmoplantar and periorificial keratoderma as the two major diagnostic features. Some authors believe that atypical cases without this standard combination may not really belong to Olmsted syndrome. Herein, we describe two familial cases with congenital nonmutilating palmoplantar and periorificial keratoderma, and discuss their similarities and differences with Olmsted syndrome.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1365-4632
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
658-65
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pubmed:meshHeading |
pubmed-meshheading:20618471-Adolescent,
pubmed-meshheading:20618471-Biopsy,
pubmed-meshheading:20618471-Child,
pubmed-meshheading:20618471-Facial Dermatoses,
pubmed-meshheading:20618471-Family Health,
pubmed-meshheading:20618471-Female,
pubmed-meshheading:20618471-Foot Dermatoses,
pubmed-meshheading:20618471-Hand Dermatoses,
pubmed-meshheading:20618471-Humans,
pubmed-meshheading:20618471-Keratoderma, Palmoplantar,
pubmed-meshheading:20618471-Siblings,
pubmed-meshheading:20618471-Syndrome
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pubmed:year |
2010
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pubmed:articleTitle |
Nonmutilating palmoplantar and periorificial kertoderma: a variant of Olmsted syndrome or a distinct entity?
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pubmed:affiliation |
Department of Dermatology, Faculty of Medicine, Zagazig University, Zagazig, Egypt. ahmadnofal5@hotmail.com
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pubmed:publicationType |
Journal Article,
Case Reports
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