Source:http://linkedlifedata.com/resource/pubmed/id/10844262
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2000-8-9
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pubmed:abstractText |
Hereditary progressive mucinous histiocytosis is an uncommon condition which to date has only been observed in women. The disease is a non-Langerhans histiocytosis with a stereotypic clinical presentation limited to the skin. The clinical, histological and genetic features of this disease differ considerably from other types of histiocytoses and overload diseases. We report the first case observed in France.
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pubmed:language |
fre
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0151-9638
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
127
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
400-4
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10844262-Disease Progression,
pubmed-meshheading:10844262-Female,
pubmed-meshheading:10844262-Histiocytosis,
pubmed-meshheading:10844262-Humans,
pubmed-meshheading:10844262-Middle Aged,
pubmed-meshheading:10844262-Pedigree,
pubmed-meshheading:10844262-Skin Diseases, Vesiculobullous
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pubmed:year |
2000
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pubmed:articleTitle |
[Hereditary progressive mucinous histiocytosis].
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pubmed:affiliation |
Service de Dermatologie, Hôpital Pasteur, 68024 Colmar Cedex, France.
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
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