Evidence map›Paper›PMID 42344785›Full record

ArticleSage open pediatrics

Early-Onset Severe Atopic Dermatitis With Hyper-IgE Overlap in a Child With a Heterozygous FLG Variant: A Case Report.

Tung Viet Cao, Anh Thi Van Nguyen, Thuy Minh Ha, Mai Thi Phuong Nguyen, Ly Ha Pham, Khiem Van Nguyen

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Article in Sage open pediatrics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Tung Viet CaoVietnam National Children's Hospital, Hanoi, Vietnam.ORCID https://orcid.org/0000-0002-7991-5638
Anh Thi Van NguyenVietnam National Children's Hospital, Hanoi, Vietnam.ORCID https://orcid.org/0000-0003-4163-466X
Thuy Minh HaUniversity of Auckland, Auckland, New Zealand.ORCID https://orcid.org/0000-0002-2256-200X
Mai Thi Phuong NguyenVietnam National Children's Hospital, Hanoi, Vietnam.ORCID https://orcid.org/0000-0002-7299-5209
Ly Ha PhamVietnam University of Traditional Medicine, Hanoi, Vietnam.ORCID https://orcid.org/0009-0001-8437-5672
Khiem Van NguyenVietnam National Children's Hospital, Hanoi, Vietnam.ORCID https://orcid.org/0000-0001-9150-253X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Markedly elevated IgE in children is an important but nonspecific clue, particularly with early-onset atopic dermatitis, eosinophilia, and infections. We report a boy who developed generalized eczema at approximately 6 months of age and was repeatedly hospitalized during infancy for severe dermatitis, prolonged diarrhea, pneumonia, acute otitis media, and Staphylococcus aureus bacteremia. Early investigations showed eosinophilia, hypoalbuminemia, rapid IgE escalation, and lymphocyte subsets not suggestive of a clear T-, B-, or NK-cell deficiency. After 12 months, no further severe infections requiring hospitalization were documented, whereas chronic severe dermatitis, eosinophilia, markedly elevated IgE, and later asthma became dominant. Whole-exome sequencing identified two FLG variants; among these, Sanger sequencing confirmed a heterozygous FLG NM_002016.2:c.6950_6957del (p.Ser2317Ter) variant. This case highlights overlaps between severe barrier-related atopic dermatitis and hyper-IgE syndrome and emphasizes longitudinal follow-up, immunological evaluation, vaccine history, genetic interpretation, and gene-environment interactions.

Indexed as

atopic dermatitischildeosinophiliafilaggrinFLGhyper-IgE syndrome

Identifiers

PMID42344785
PMCPMC13287414

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