Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.

Staple L; Andrews T; McDonald-McGinn D; Zackai E; Sullivan KE

doi:10.1111/j.1399-3038.2005.00259.x

Abstract

Humoral immunodeficiencies have a recognized association with atopy. This study investigated the association of a T-cell disorder (chromosome 22q11.2 deletion) and a neutrophil disorder [chronic granulomatous disease (CGD)] with asthma, eczema, and rhinitis using a standardized survey instrument. Patients were recruited from either a national referral center (chromosome 22q11.2 deletion syndrome) or from a registry (CGD). Controls consisted of siblings of patients. Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) was found to be significantly associated with both eczema and asthma but not allergic rhinitis. CGD was not found to be significantly associated with atopic diseases.

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References

Articles referenced by this article (37)

Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder.
Grimbacher B, Holland SM, Gallin JI, Greenberg F, Hill SC, Malech HL, Miller JA, O'Connell AC, Puck JM
N Engl J Med, (9):692-702 1999
MED: 10053178
A multiinstitutional survey of the Wiskott-Aldrich syndrome.
Sullivan KE, Mullen CA, Blaese RM, Winkelstein JA
J Pediatr, (6 Pt 1):876-885 1994
MED: 7996359
Characterization of immune function and analysis of RAG gene mutations in Omenn syndrome and related disorders.
Wada T, Takei K, Kudo M, Shimura S, Kasahara Y, Koizumi S, Kawa-Ha K, Ishida Y, Imashuku S, Seki H, Yachie A
Clin Exp Immunol, (1):148-155 2000
MED: 10606976
IgA deficiency: clinical correlates and responses to pneumococcal vaccine.
Edwards E, Razvi S, Cunningham-Rundles C
Clin Immunol, (1):93-97 2004
MED: 15093556
Clinical manifestations in selective IgA deficiency in childhood. A follow-up report.
De Laat PC, Weemaes CM, Gonera R, Van Munster PJ, Bakkeren JA, Stoelinga GB
Acta Paediatr Scand, (8-9):798-804 1991
MED: 1957599
Familial selective IgA deficiency with circulating anti-IgA antibodies: a distinct group of patients?
de Laat PC, Weemaes CM, Bakkeren JA, van den Brandt FC, van Lith TG, de Graaf R, van Munster PJ, Stoelinga GB
Clin Immunol Immunopathol, (1):92-101 1991
MED: 1983972
Comparison of the frequency of atopic diseases in children with severe and partial IgA deficiency.
Plebani A, Monafo V, Ugazio AG, Monti C, Avanzini MA, Massimi P, Burgio GR
Int Arch Allergy Appl Immunol, (3-4):485-486 1987
MED: 3570519
Immediate hypersensitivity in adults with IgG deficiency and recurrent respiratory infections.
Popa V, Nagy SM Jr
Ann Allergy Asthma Immunol, (6):567-573 1999
MED: 10400485
Deficiency of IgG4 in children: association of isolated IgG4 deficiency with recurrent respiratory tract infection.
Moss RB, Carmack MA, Esrig S
J Pediatr, (1):16-21 1992
MED: 1731015
Ig isotypes deficiency caused by gene deletions.
Carbonara AO, Demarchi M
Monogr Allergy, 13-17 1986
MED: 3773904

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Grant ID: M01 RR00240
14 publications

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Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.

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Abstract

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References

Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder.

A multiinstitutional survey of the Wiskott-Aldrich syndrome.

Characterization of immune function and analysis of RAG gene mutations in Omenn syndrome and related disorders.

IgA deficiency: clinical correlates and responses to pneumococcal vaccine.

Clinical manifestations in selective IgA deficiency in childhood. A follow-up report.

Familial selective IgA deficiency with circulating anti-IgA antibodies: a distinct group of patients?

Comparison of the frequency of atopic diseases in children with severe and partial IgA deficiency.

Immediate hypersensitivity in adults with IgG deficiency and recurrent respiratory infections.

Deficiency of IgG4 in children: association of isolated IgG4 deficiency with recurrent respiratory tract infection.

Ig isotypes deficiency caused by gene deletions.

Citations & impact

Impact metrics

Citations of article over time

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Smart citations by scite.ai
Explore citation contexts and check if this article has been supported or disputed.
https://scite.ai/reports/10.1111/j.1399-3038.2005.00259.x

Article citations

Atopic manifestations of inborn errors of immunity.

Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development.

Beyond Bone: Infectious Diseases and Immunity in Parathyroid Disorders.

Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome.

Successful treatment of severe allergic asthma with omalizumab in a girl with DiGeorge syndrome.

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Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.

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