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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1978-8-28
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pubmed:abstractText |
We describe a patient in whom selective IgA deficiency and homozygous alpha1-antitrypsin deficiency were discovered. Clinically, the patient suffered from chronic sinopulmonary infections, destructive emphysema, and bronchiectasis. The interrelation of IgA and alpha1-antitrypsin was studied. Twenty-three alpha1-antitrypsin-deficient sera were screened for IgA deficiency. None of these sera were deficient in IgA. Fifteen IgA-deficient sera were screened for alpha1-antitrypsin deficiency. In this group, three patients were found to have variant alpha1-antitrypsin phenotypes. Respiratory infections were a prominent complaint in all three of these patients, with bronchiectasis in two patients. We believe that the combination of IgA and alpha1-antitrypsin deficiencies should be considered in the evaluation of any patient with idiopathic bronchiectasis.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
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pubmed:issn |
0012-3692
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
73
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
885-6
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pubmed:dateRevised |
2009-2-17
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pubmed:meshHeading |
pubmed-meshheading:306913-Bronchiectasis,
pubmed-meshheading:306913-Dysgammaglobulinemia,
pubmed-meshheading:306913-Humans,
pubmed-meshheading:306913-Immunoglobulin A,
pubmed-meshheading:306913-Male,
pubmed-meshheading:306913-Middle Aged,
pubmed-meshheading:306913-Phenotype,
pubmed-meshheading:306913-Pulmonary Emphysema,
pubmed-meshheading:306913-Respiratory Tract Infections,
pubmed-meshheading:306913-alpha 1-Antitrypsin Deficiency
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pubmed:year |
1978
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pubmed:articleTitle |
Selective IgA deficiency and Pi ZZ-antitrypsin deficiency. Association with recurrent sinopulmonary infections, emphysema, and bronchiectasis.
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pubmed:publicationType |
Journal Article,
Case Reports
|