Blazina Štefan, Ihan Alojz, Lovrečić Luca, Hovnik Tinka
Department of Allergy, Rheumatology and Clinical Immunology, Children's Hospital Ljubljana, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Institute of Microbiology and Immunology, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Am J Med Genet A. 2016 Dec;170(12):3237-3240. doi: 10.1002/ajmg.a.37859. Epub 2016 Sep 8.
Antibody deficiency is common finding in patients with Jacobsen syndrome (JS). In addition, there have been few reports of T-cell defects in this condition, possibly because most of the reported patients have not been specifically evaluated for T-cell function. In this article, we present a child with an 11q deletion and combined immunodeficiency and we perform a literature overview on immunodeficiency in JS. Our patient presented with recurrent bacterial and prolonged viral infections involving the respiratory system, as well as other classic features of the syndrome. In addition to low IgM, IgG4, and B-cells, also low recent thymic emigrants, helper and naïve T-cells were found. We propose that patients with Jacobsen syndrome need thorough immunological evaluations as T-cell dysfunction might be more prevalent than previously reported. Patients with infections consistent with T-cell defects should be classified as having combined immunodeficiency. © 2016 Wiley Periodicals, Inc.
J Clin Immunol. 2014-1
Genes (Basel). 2021-7-31
Genet Mol Res. 2016-7-14
Am J Med Genet C Semin Med Genet. 2015-9
Clin Case Rep. 2023-6-15
J Cardiovasc Dev Dis. 2022-12-24
Genes (Basel). 2021-7-31
Ital J Pediatr. 2021-7-1
Cold Spring Harb Mol Case Stud. 2019-6-3