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Selective IgA deficiency: clinical and immunological evaluation of 50 pediatric patients.

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.
AuthorsG R Burgio, M Duse, V Monafo, A Ascione, L Nespoli
JournalEuropean journal of pediatrics (Eur J Pediatr) Vol. 133 Issue 2 Pg. 101-6 (Mar 1980) ISSN: 0340-6199 [Print] Germany
PMID6444875 (Publication Type: Journal Article)
Chemical References
  • Immunoglobulin A
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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