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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1976-4-1
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pubmed:abstractText |
In a boy initially diagnosed as X-linked hypogammaglobulinemia, the later clinical and analytical course and the application of new immunological techniques led to the new diagnosis of common variable immunodeficiency. The patient shows panhypogammaglobulinemia, a scarce number of plasma cells with a normal number of precursors and circulating B lymphocytes with membrane bound immunoglobulins and C3 receptors. Delayed hypersensitivity is absent despite normal amount of circulating T lymphocytes which were able to transform when stimulated by PHA. The anergy seems primary and not related to the clinical malnutrition. The authors make a differential diagnosis between both illnesses as a tentative pathogenetic interpretation of B cell development arrest.
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pubmed:language |
spa
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0302-4342
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
677-84
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1211695-Agammaglobulinemia,
pubmed-meshheading:1211695-Child,
pubmed-meshheading:1211695-Diagnosis, Differential,
pubmed-meshheading:1211695-Humans,
pubmed-meshheading:1211695-Immunoglobulins,
pubmed-meshheading:1211695-Immunologic Deficiency Syndromes,
pubmed-meshheading:1211695-Male,
pubmed-meshheading:1211695-Pedigree,
pubmed-meshheading:1211695-Sex Factors
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pubmed:articleTitle |
[Common variable immunodeficiency (author's transl)].
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
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