Clinical and Immunological Features of a Large DiGeorge Syndrome Cohort

CD4 lymphopenia was more common than CD8 lymphopenia. Normal/high CD8 + and NK cell counts were remarkable. Increased CD8+ TEMRA cells seem to indicate peripheral homeostatic proliferation following viral infections. Low serum IgA correlated with low RTE% and impaired T-cell function. DGS severity markers include hypocalcemia, congenital cardiac anomaly, and T-cell lymphopenia.

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Publication Details

Journal
Journal of Clinical Immunology
Published
2025-06-03
DOI
https://doi.org/10.1007/s10875-025-01884-0
Citations
3
Primary Topic
Congenital heart defects research
Type
article
Field-Weighted Citation Impact
2.42

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article

Clinical and Immunological Features of a Large DiGeorge Syndrome Cohort

Pelin Özlem Şimşek‐Kiper, Gülen Eda Ütine, İlhan Tezcan, Deniz Çağdaş et al.
3 citations
Journal of Clinical Immunology
Congenital heart defects research
2.42
article

Clinical and Immunological Features of a Large DiGeorge Syndrome Cohort

Pelin Özlem Şimşek‐Kiper, Gülen Eda Ütine, İlhan Tezcan, Deniz Çağdaş, Merve Kaşıkçı, Merve Süleyman
article en
3 citations

Abstract

CD4 lymphopenia was more common than CD8 lymphopenia. Normal/high CD8 + and NK cell counts were remarkable. Increased CD8+ TEMRA cells seem to indicate peripheral homeostatic proliferation following viral infections. Low serum IgA correlated with low RTE% and impaired T-cell function. DGS severity markers include hypocalcemia, congenital cardiac anomaly, and T-cell lymphopenia.

Journal of Clinical ImmunologyVol. 45(1)
Hacettepe University Hospital (TR), Hacettepe University (TR)
Hacettepe Üniversitesi
Openalex Percentile: Top 11%
Congenital heart defects research
2.42
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Clinical and Immunological Features of a Large DiGeorge Syndrome Cohort — Pelin Özlem Şimşek‐Kiper, Gülen Eda Ütine, et al. · Journal of Clinical Immunology (2025) | TGRS Research Map | TGRS