We report the first detailed immunological characterization of a DEGCAGS patient, showing that biallelic ZNF699 loss-of-function variants can cause syndromic combined immunodeficiency and that DNA methylation profiling improves diagnostic precision in selected inborn errors of immunity.

A novel ZNF699 mutation in a patient with DEGCAGS syndrome and severe B cell depletion / Giardino, G., Romano, R., Squeo, G.M., Toriello, E., De Rosa, A., Ammendola, A., Gemma, G., Rzasa, J., Kerkhof, J., Di Venere, E., Cantelli, M., Cirillo, E., Nigro, V., Sadikovic, B., Pignata, C., Merla, G.. - In: JOURNAL OF HUMAN IMMUNITY. - ISSN 3065-8993. - 2:5(2026). [10.70962/jhi.20250204]

A novel ZNF699 mutation in a patient with DEGCAGS syndrome and severe B cell depletion

Giardino, Giuliana;Squeo, Gabriella Maria;Toriello, Elisabetta;Gemma, Giorgia;di Venere, Eleonora;Cantelli, Mariateresa;Nigro, Vincenzo;Pignata, Claudio;Merla, Giuseppe
2026

Abstract

We report the first detailed immunological characterization of a DEGCAGS patient, showing that biallelic ZNF699 loss-of-function variants can cause syndromic combined immunodeficiency and that DNA methylation profiling improves diagnostic precision in selected inborn errors of immunity.
2026
A novel ZNF699 mutation in a patient with DEGCAGS syndrome and severe B cell depletion / Giardino, G., Romano, R., Squeo, G.M., Toriello, E., De Rosa, A., Ammendola, A., Gemma, G., Rzasa, J., Kerkhof, J., Di Venere, E., Cantelli, M., Cirillo, E., Nigro, V., Sadikovic, B., Pignata, C., Merla, G.. - In: JOURNAL OF HUMAN IMMUNITY. - ISSN 3065-8993. - 2:5(2026). [10.70962/jhi.20250204]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/1072918
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