Abstract |
Fifty children with IgA deficiency were folllowed for 1 to 4 years from 1975 to 1978. Thirty-five had complete deficiency of serum IgA (less than 2.5 IU/ml) and 15 partial deficiency (serum IgA below the 10th centile for age). Patients with another associated immunodeficiency, such as ataxia-telangiectasia, were not included. Most children with complete deficiency of IgA had recurrent respiratory and/or gastrointestinal infections, about half with onset in the first year of life, while partial deficiency of IgA has probably little if any importance for anti-infectious immunity but is important in the pathogenesis of atopy. Atopic diseases were frequent in both groups. Chromosomal abnormalities were found in 2 patients: trisomy 21 in one and in the other a ring chromosome 18. No important defects in cellular immunity were detected but some isolated, borderline abnormalities were often present.
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Authors | G R Burgio, M Duse, V Monafo, A Ascione, L Nespoli |
Journal | European journal of pediatrics
(Eur J Pediatr)
Vol. 133
Issue 2
Pg. 101-6
(Mar 1980)
ISSN: 0340-6199 [Print] Germany |
PMID | 6444875
(Publication Type: Journal Article)
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Chemical References |
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Topics |
- Child
- Child, Preschool
- Chromosome Aberrations
(immunology)
- Chromosome Disorders
- Chromosomes, Human, 16-18
- Down Syndrome
(immunology)
- Dysgammaglobulinemia
(immunology)
- Female
- Gastroenteritis
(immunology)
- Humans
- IgA Deficiency
- Immunity, Cellular
- Immunoglobulin A
(analysis)
- Infant
- Male
- Recurrence
- Respiratory Tract Infections
(immunology)
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