1970
DOI: 10.1016/b978-0-08-015566-1.50017-4
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The Genetics of IgA Deficiency

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1972
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Cited by 4 publications
(3 citation statements)
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“…Recently, simultaneous absence of IgG1, IgG2, IgG4, and IgAl subclasses was found, the deletion of a block of 'y -al -72 - 4 structural genes was postulated and confirmed by DNA analysis (26,27). As far as IgA deficiency is concerned, autosomal dominant and recessive modes of inheritance have been described (3)(4)(5). The finding of a normal percentage of lymphocytes carrying IgA in cases of selective IgA deficiency argues against a possible defect of structural a-genes (9).…”
Section: Resultsmentioning
confidence: 99%
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“…Recently, simultaneous absence of IgG1, IgG2, IgG4, and IgAl subclasses was found, the deletion of a block of 'y -al -72 - 4 structural genes was postulated and confirmed by DNA analysis (26,27). As far as IgA deficiency is concerned, autosomal dominant and recessive modes of inheritance have been described (3)(4)(5). The finding of a normal percentage of lymphocytes carrying IgA in cases of selective IgA deficiency argues against a possible defect of structural a-genes (9).…”
Section: Resultsmentioning
confidence: 99%
“…Several reports have been published on the familial occurrence of Ig deficiencies (1)(2)(3)(4)(5)(6).…”
Section: Introductionmentioning
confidence: 99%
“…Since the initial description of isolated IgA deficiency in 2 healthy men [20], a great deal of attention has been focused on the genetics of this deficiency [7,19] and on the association of this type of immunological deficiency and disease [1]. In population studies, the frequency of selective IgA deficiency has been found to vary from 1/100 to 1/3,000 (table I).…”
Section: Introductionmentioning
confidence: 99%