Genetic mutations in lymphocytic variant of hypereosinophilic syndrome: study of five siblings
IntroductionLymphocytic variant hypereosinophilic syndrome (L-HES) is a rare subtype of hypereosinophilic syndrome driven by aberrant T-cell clones that promote eosinophilia through interleukin-5 (IL-5) overproduction. While clonal T-cell receptor (TCR) rearrangements are a hallmark, the underlying...
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| Päätekijät: | , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2025-12-01
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| Sarja: | Frontiers in Medicine |
| Aiheet: | |
| Linkit: | https://www.frontiersin.org/articles/10.3389/fmed.2025.1679484/full |
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