ArticleJournal of clinical medicine2026
Chung-Jansen Syndrome in a Young Woman with a PHIP Variant: Severe Obesity, Intellectual Disability, and Endocrine Abnormalities.
Francesco Donno, Federica Bianco, Roberta Schininà, Rita Selvatici, Giuseppina Stoico, Alessandra Ferlini, Alberto Gobbo, Maria Chiara Zatelli, Stefania Bigoni, Maria Rosaria Ambrosio
Abstract readCase Reports
In one paragraphArticle in Journal of clinical medicine, 2026. 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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0cells of the map it votes in
0citing papers in PubMed
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What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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 registryThe trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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 literatureWho cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors and funding
10 authors.
Francesco DonnoSection of Endocrinology, Geriatrics and Internal Medicine, Department of Medical Sciences, University of Ferrara, 44124 Ferrara, Italy.ORCID 0009-0000-6021-421X Federica BiancoSection of Endocrinology, Geriatrics and Internal Medicine, Department of Medical Sciences, University of Ferrara, 44124 Ferrara, Italy.ORCID 0009-0006-6353-0625 Roberta SchininàMedical Genetics Unit, Department of Medical Science and Department of Mother and Child, Ferrara University and Ferrara University Hospital, 44124 Ferrara, Italy.
Rita SelvaticiMedical Genetics Unit, Department of Medical Science and Department of Mother and Child, Ferrara University and Ferrara University Hospital, 44124 Ferrara, Italy.ORCID 0000-0002-3099-0100 Giuseppina StoicoMedical Genetics Unit, Department of Medical Science and Department of Mother and Child, Ferrara University and Ferrara University Hospital, 44124 Ferrara, Italy.
Alessandra FerliniMedical Genetics Unit, Department of Medical Science and Department of Mother and Child, Ferrara University and Ferrara University Hospital, 44124 Ferrara, Italy.ORCID 0000-0001-8385-9870 Alberto GobboSection of Endocrinology, Geriatrics and Internal Medicine, Department of Medical Sciences, University of Ferrara, 44124 Ferrara, Italy.ORCID 0000-0002-4010-2154 Maria Chiara ZatelliSection of Endocrinology, Geriatrics and Internal Medicine, Department of Medical Sciences, University of Ferrara, 44124 Ferrara, Italy.ORCID 0000-0001-8408-7796 Stefania BigoniMedical Genetics Unit, Department of Medical Science and Department of Mother and Child, Ferrara University and Ferrara University Hospital, 44124 Ferrara, Italy.ORCID 0000-0003-0336-7097 Maria Rosaria AmbrosioSection of Endocrinology, Geriatrics and Internal Medicine, Department of Medical Sciences, University of Ferrara, 44124 Ferrara, Italy.ORCID 0000-0002-7911-9770 Funding
University of Ferrara FAR2025 and FAR2026
6 · The paper itselfAbstract
PubMed holds no abstract for this paper.
Indexed as
behavioural disturbancescase reportendocrine dysfunctionsfacial dysmorphismsnext generation sequencing
Identifiers
PMID42355777
PMCPMC13301996
What OpenQuestion holds
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