ArticleCureus2025
Hyperactive Catatonia in an Adolescent With Prader-Willi Syndrome.
Article in Cureus, 2025. 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.
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0 citing papers in PubMed.
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Catatonia, a neuropsychiatric syndrome, has been increasingly recognized as a possible complication of Prader-Willi syndrome (PWS). There is limited research surrounding catatonia and its sequelae in PWS. Given the scarcity and severity of catatonia in pediatric age, there is a need to expand on the available literature. We present a case of hyperactive catatonia in an adolescent with PWS. After obtaining a thorough history, we followed her progression from motor symptoms to developing psychotic features. Although her presentation required multiple doses of lorazepam, it was shown to be consistently effective in treating her catatonia during her hospital stay.
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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.