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Decreased T helper 1 cell function underlies recurrent sinopulmonary infections in the 17q12 deletion syndrome

Background The 17q12 deletion syndrome (17q12DS) is a heterozygous deletion of a 1.4 megabase‒spanning DNA sequence on chromosome 17.

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How this was derived

Indexed from **pmc** on 2026-11-13 (relevance 1.00, tier peer_reviewed).

Generated 2026-11-13, last changed yesterday. Dedup key newdoc:378. The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.

Evidence (1 quote)

Decreased T helper 1 cell function underlies recurrent sinopulmonary infections in the 17q12 deletion syndrome peer_reviewed · published 2025-01-01 · live page
28 To the best of our knowledge, this study is the first report to indicate a decreased frequency of IFN-γ + CD4 + T cells in individuals with 17q12DS.

Supporting documents (1)

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Decreased T helper 1 cell function underlies recurrent sinopulmonar... pmc 2025-01-01 yesterday 1.00