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11q terminal deletion and combined immunodeficiency (Jacobsen syndrome): Case report and literature review on immunodeficiency in Jacobsen syndrome.

作者信息

Blazina Štefan, Ihan Alojz, Lovrečić Luca, Hovnik Tinka

机构信息

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.

出版信息

Am J Med Genet A. 2016 Dec;170(12):3237-3240. doi: 10.1002/ajmg.a.37859. Epub 2016 Sep 8.


DOI:10.1002/ajmg.a.37859
PMID:27605496
Abstract

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.

摘要

相似文献

[1]
11q terminal deletion and combined immunodeficiency (Jacobsen syndrome): Case report and literature review on immunodeficiency in Jacobsen syndrome.

Am J Med Genet A. 2016-12

[2]
The 11q Terminal Deletion Disorder Jacobsen Syndrome is a Syndromic Primary Immunodeficiency.

J Clin Immunol. 2015-11

[3]
Patients with Chromosome 11q Deletions Are Characterized by Inborn Errors of Immunity Involving both B and T Lymphocytes.

J Clin Immunol. 2022-10

[4]
A small terminal deletion 11q in a boy without Jacobsen syndrome: narrowing the critical region for the 11q Jacobsen syndrome phenotype.

Am J Med Genet A. 2012-3

[5]
Terminal deletion of 11q with significant late-onset combined immune deficiency.

J Clin Immunol. 2014-1

[6]
Case report: gene deletion associated with a low number of recent thymic emigrants in three patients with Jacobsen syndrome.

Front Immunol. 2022

[7]
Immune Deficiency in Jacobsen Syndrome: Molecular and Phenotypic Characterization.

Genes (Basel). 2021-7-31

[8]
De novo interstitial deletion in the long arm of chromosome 11: a case report.

Genet Mol Res. 2016-7-14

[9]
Jacobsen syndrome: Advances in our knowledge of phenotype and genotype.

Am J Med Genet C Semin Med Genet. 2015-9

[10]
11q24.2q24.3 microdeletion in two families presenting features of Jacobsen syndrome, without intellectual disability: Role of FLI1, ETS1, and SENCR long noncoding RNA.

Am J Med Genet A. 2019-3-19

引用本文的文献

[1]
Recurrent pneumonia in a child with Jacobsen syndrome and common variable immune deficiency.

Clin Case Rep. 2023-6-15

[2]
Jacobsen Syndrome with Hypoplastic Left Heart Syndrome: Outcome after Cardiac Transplantation.

J Cardiovasc Dev Dis. 2022-12-24

[3]
Case report: gene deletion associated with a low number of recent thymic emigrants in three patients with Jacobsen syndrome.

Front Immunol. 2022

[4]
Patients with Chromosome 11q Deletions Are Characterized by Inborn Errors of Immunity Involving both B and T Lymphocytes.

J Clin Immunol. 2022-10

[5]
Immune Deficiency in Jacobsen Syndrome: Molecular and Phenotypic Characterization.

Genes (Basel). 2021-7-31

[6]
Jacobsen syndrome and neonatal bleeding: report on two unrelated patients.

Ital J Pediatr. 2021-7-1

[7]
Ultrasonographic findings and prenatal diagnosis of Jacobsen syndrome: A case report and review of the literature.

Medicine (Baltimore). 2020-1

[8]
Partial Jacobsen syndrome phenotype in a patient with a de novo frameshift mutation in the ETS1 transcription factor.

Cold Spring Harb Mol Case Stud. 2019-6-3

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