Linked Life Data

7611799

Source:http://linkedlifedata.com/resource/pubmed/id/7611799

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
1995-8-14
pubmed:abstractText
Cutaneous necrosis of the proximal lower extremities in a patient with end-stage renal disease is the classic presentation of calciphylaxis, an untreatable, rare, generally fatal necrotizing cutaneous syndrome. Type 1 primary hyperoxaluria (PH-1) usually presents in childhood with recurrent urolithiasis. Since enzymatic studies to confirm the metabolic defect are now available, some cases of idiopathic renal failure in adulthood have been shown to be caused by PH-1. These patients may develop vascular oxalate deposits resulting in livedo reticularis and distal acral vascular insufficiency.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0003-987X
pubmed:author
pubmed:issnType
Print
pubmed:volume
131
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
821-3
pubmed:dateRevised
2008-3-17
pubmed:meshHeading
pubmed:year
1995
pubmed:articleTitle
Fatal cutaneous necrosis mimicking calciphylaxis in a patient with type 1 primary hyperoxaluria.
pubmed:affiliation
Department of Dermatology, Case Western Reserve University, Cleveland, Ohio, USA.
pubmed:publicationType
Journal Article, Case Reports