ArticleCureus2026
Prader-Willi Syndrome Presenting With Early Infantile Hypotonia: A Case Report.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
The 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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Prader-Willi syndrome (PWS) is a genetic disorder resulting from the loss of paternally expressed genes on chromosome 15q11.2-15q13.3. It is characterized by distinct clinical features and multisystem involvement, including endocrine, neurodevelopmental, and metabolic abnormalities. Early diagnosis can be challenging because clinical manifestations in infancy are often subtle; therefore, molecular testing is essential for confirmation. This report describes a one-year-old child newly diagnosed with PWS, aiming to highlight the clinical presentation and correlate the findings with current genetic and phenotypic evidence.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.