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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1982-12-16
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pubmed:abstractText |
Alpha 1 antitrypsin phenotypes and serum levels are presented for a family in which two brothers have Weber Christian disease and alpha 1 antitrypsin (PI) Z phenotypes. Clinical histories are described for these two men. A younger brother has the PI Z phenotype but does not have the disease, indicating that additional genetic and/or environmental factors contribute to the pathogenesis of Weber Christian disease. However, the two cases described provide additional evidence for a relationship between alpha 1 antitrypsin deficiency and the development of symptoms.
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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 |
Sep
|
pubmed:issn |
0148-7299
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
13
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
57-62
|
pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:6982619-Adult,
pubmed-meshheading:6982619-Female,
pubmed-meshheading:6982619-Humans,
pubmed-meshheading:6982619-Male,
pubmed-meshheading:6982619-Panniculitis, Nodular Nonsuppurative,
pubmed-meshheading:6982619-Pedigree,
pubmed-meshheading:6982619-Phenotype,
pubmed-meshheading:6982619-alpha 1-Antitrypsin Deficiency
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pubmed:year |
1982
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pubmed:articleTitle |
Genetic study of a family with two members with Weber Christian disease (panniculitis) and alpha 1 antitrypsin deficiency.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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