Linked Life Data

6332492

Source:http://linkedlifedata.com/resource/pubmed/id/6332492

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1984-10-15
pubmed:abstractText
Behçet disease is an uncommon systemic process that appears most often in the third or fourth decade of life. It is characterized by recurrent orogenital ulcers and ocular and cutaneous inflammatory lesions. Cardiovascular involvement, which may be arterial or venous, is rare but carries a particularly poor prognosis. Three new cases are reported, and they are characterized by typical orogenital and cutaneous manifestations and associated severe vasculitis. The arterial findings in these cases were occlusions and aneurysms and pseudoaneurysms of the aorta and pulmonary, brachiocephalic, and visceral arteries. From these cases and those previously reported, arterial involvement in Behçet disease can be characterized by saccular aneurysms or occlusions of multiple large vessels in young adults.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0361-803X
pubmed:author
pubmed:issnType
Print
pubmed:volume
143
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
821-5
pubmed:dateRevised
2008-2-15
pubmed:meshHeading
pubmed:year
1984
pubmed:articleTitle
Arterial manifestations of Behçet disease.
pubmed:publicationType
Journal Article, Case Reports