Increased prevalence of immunoglobulin a deficiency in patients with the chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)

Clinical and Diagnostic Laboratory Immunology

Volumn 5, Issue 3, 1998, Pages 415-417

  Smith, Christopher A ^a   Driscoll, Deborah A ^b   Emanuel, Beverly S ^a   McDonald McGinn, Donna M ^a   Zackai, Elaine H ^a   Sullivan, Kathleen E ^a  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

IMMUNOGLOBULIN A;

CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL ARTICLE; DIGEORGE SYNDROME; HUMAN; HUMORAL IMMUNE DEFICIENCY; IMMUNOGLOBULIN A DEFICIENCY; PREVALENCE; PRIORITY JOURNAL; RISK; SHORT SURVEY;

EID: 0031833947     PISSN: 1071412X     EISSN: None     Source Type: Journal    
DOI: 10.1128/cdli.5.3.415-417.1998     Document Type: Short Survey

References (22)

1. Bastian, J., S. Law, L. Vogler, A. Lawton, H. Herrod, S. Anderson, S. Horowitz, and R. Hong. 1989. Prediction of persistent immunodeficiency in the DiGeorge anomaly. J. Pediatr. 115:391-396.
2. Buckley, R. H. 1993. Primary immunodeficiency diseases, p. 1353-1374. In W. E. Paul (ed.), Fundamental immunology, 3rd ed. Raven Press, New York, N.Y.
3. Cassidy, J. T., and G. L. Nordby. 1975. Human serum immunoglobulin concentrations: prevalence of immunoglobulin deficiencies. J. Allergy Clin. Immunol. 55:35-48.
4. Clark, J. A., P. A. Callicoat, N. A. Brenner, C. A. Bradley, and D. M. Smith. 1983. Selective IgA deficiency in blood donors. Am. J. Clin. Pathol. 80:210-213.
5. Conley, M. E., J. B. Beckwith, J. F. K. Mancer, and L. Tenckhoff. 1979. The spectrum of DiGeorge syndrome. J. Pediatr. 94:883-890.
6. Comans-Bitter, W. M., R. de Groot, and J. M. van Dongen. 1996. Immunophenotyping of blood lymphocytes in childhood. J. Pediatr. 130:388-393.
7. Cunningham-Rundles, C. 1996. Diseases of the IgA system. p. 423-442. In E. R. Stichm (ed.). Immunologic disorders in infants and children. W. B. Saunders, Philadelphia. Pa.
8. Driscoll, D. A., M. L. Budarf, and B. S. Emanuel. 1992. A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11. Am. J. Hum. Genet. 50:924-933.
9. Driscoll, D. A., M. Li, P. Chien, S. Capuano, E. H. Zackai, D. M. McDonald-McGinn, K. M. Christensen, B. F. Cuneo, H. M. Saal, R. Gold, E. B. Spector, B. S. Emanuel, and M. L. Budarf. 1995. Familial 22q11 deletions: phenotypic variability and determination of deletion boundaries by FISH. Am. J. Hum. Genet. 57:A163.
10. Holt, P. D. J., N. P. Tandy, and D. J. Anstee. 1977. Screening of blood donors for IgA deficiency: a study of the donor population of southwest England. J. Clin. Pathol. 30:1007-1010.
11. Junker, A. K., and D. A. Driscoll. 1995. Humoral immunity in DiGeorge syndrome. J. Pediatr. 127:231-237.
12. Kelley, R. I., E. H. Zackai, B. S. Emanuel, M. Kistenmacher, F. Greenberg, and H. H. Punnett. 1982. The association of the DiGeorge anomalad with partial monosomy of chromosome 22. J. Pediatr. 101:197 200.
13. Lawton, A. R., and D. S. Hummel. 1996. Primary antibody deficiencies, p. 621-626. In R. R. Rich (ed.), Clinical immunology principles and practice. Mosby-Year Book, Inc., St. Louis, Mo.
14. Miranda, J. L. G., A. O. Gomez, H. V. Ansedes, N. R. Torres, C. G. Espinosa, C. Cortabarria, and G. S. Salgado. 1983. Monosomy 22 with humoral immunodeficiency: is there an immunoglobulin chain deficit? J. Med. Genet. 20:69-72.
15. Ropars, C., A. Muller, N. Paint, D. Beige, and G. Avenard. 1982. Large scale detection of IgA deficient blood donors. J. Immunol. Methods 54:183-189.
16. Stiehm, E. R., and H. H. Fudenberg. 1966. Serum levels of immune globulins in health and disease: a survey. Pediatrics 37:715-727.
17. Strober, W., and M. C. Sneller. 1991. IgA deficiency. Ann. Allergy 66:363-375.
18. Sullivan, K., D. McDonald-McGinn, D. Driscoll, L. Reed, B. S. Emanuel, E. Zackai, B. H. Athreya, and G. Keenan. 1997. Juvenile rheumatoid arthritislike polyarthritis in chromosome 22q11.2 deletion syndrome (DiGeorge anomalad/velocardiofacial syndrome/conotruncal anomaly face syndrome). Arthritis Rheum. 40:430-436.
19. Sullivan, K. E., A. F. Jawad, P. Randall, D. A. Driscoll, B. S. Emanuel, D. M. McDonald-McGinn, and E. H. Zackai. 1998. Lack of correlation between impaired T cell production, immunodeficiency and other phenotypic features in chromosome 22q11.2 deletions syndrome (DiGeorge syndrome/Velocardiofacial syndrome). Clin. Immunol. Immunopathol. 86:141-146.
20. Taalman, R. D. F. M., C. M. R. Weemaes, T. W. J. Hustinx, J. M. J. C. Scheres, J. M. E. Clement, and G. B. A. Stoelinga. 1987. Chromosome studies in IgA-deficient patients. Clin. Genet. 32:81-87.
21. Vyas, G. N., H. A. Perkins, and H. H. Fudenberg. 1968. Anaphylactoid transfusion reactions associated with anti-IgA. Lancet ii:312-315.
22. Wells, J. V., M. P. McNally, and M. A. King. 1980. Selective IgA deficiency in Australian blood donors. Aust. N. Z. J. Med. 10:410-413.