rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
8
|
pubmed:dateCreated |
1996-3-1
|
pubmed:abstractText |
There are two hereditary forms of primary telangiectasia with a totally opposite prognosis. In Rendu-Osler disease, also called hereditary haemorrhagic telangiectasia, there is a major risk of severe haemorrhage in adults. In benign hereditary telangiectasia there is no such risk.
|
pubmed:language |
fre
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0151-9638
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
122
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
517-20
|
pubmed:dateRevised |
2010-3-24
|
pubmed:meshHeading |
pubmed-meshheading:8572491-Child,
pubmed-meshheading:8572491-Child, Preschool,
pubmed-meshheading:8572491-Diagnosis, Differential,
pubmed-meshheading:8572491-Humans,
pubmed-meshheading:8572491-Male,
pubmed-meshheading:8572491-Microscopy, Electron,
pubmed-meshheading:8572491-Prognosis,
pubmed-meshheading:8572491-Skin,
pubmed-meshheading:8572491-Telangiectasia, Hereditary Hemorrhagic,
pubmed-meshheading:8572491-Telangiectasis
|
pubmed:year |
1995
|
pubmed:articleTitle |
[Ultrastructural study of hereditary benign telangiectasia. Differential diagnosis from Osler Rendu disease].
|
pubmed:affiliation |
Département d'Histologie, Faculté de Médecine Lariboisière-Saint-Louis, Paris.
|
pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|