Genetic Syndromic Immunodeficiencies with Antibody Defects
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This article reviews the major syndromic immunodeficiencies with significant antibody defects, many of which may require intravenous immunogammaglobulin therapy. The authors define syndromic immunodeficiency as an illness associated with a characteristic group of phenotypic abnormalities or laboratory features that comprise a recognizable syndrome. Many are familial with a defined inheritance pattern. Immunodeficiency may not be a major part of the illness and may not be present in all patients; thus, these conditions differ from primary immunodeficiency syndromes, in which immune abnormalities are a consistent and prominent feature of their disease.
Evaluation of immunological abnormalities in patients with rare syndromes.
Gul Y, Kapakli H, Erol Aytekin S, Guner S, Keles S, Zamani A Cent Eur J Immunol. 2023; 47(4):299-307.
PMID: 36817395 PMC: 9901257. DOI: 10.5114/ceji.2022.124080.
Bogaert D, Dullaers M, Kuehn H, Leroy B, Niemela J, De Wilde H Sci Rep. 2017; 7(1):3702.
PMID: 28623346 PMC: 5473876. DOI: 10.1038/s41598-017-02434-4.
The 11q Terminal Deletion Disorder Jacobsen Syndrome is a Syndromic Primary Immunodeficiency.
Dalm V, Driessen G, Barendregt B, van Hagen P, van der Burg M J Clin Immunol. 2015; 35(8):761-8.
PMID: 26566921 PMC: 4659842. DOI: 10.1007/s10875-015-0211-z.
Educational paper: syndromic forms of primary immunodeficiency.
Kersseboom R, Brooks A, Weemaes C Eur J Pediatr. 2011; 170(3):295-308.
PMID: 21337117 PMC: 3068525. DOI: 10.1007/s00431-011-1396-7.