ArticleCureus2025
Hidden Burden of Lipid Accumulation: A Clinical Case of Niemann-Pick Disease.
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
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
We showcase a 29-year-old man who had been previously diagnosed with hypertriglyceridemia. He presented with vague symptoms of generalized weakness, headache, and a feeling of hotness. Investigations revealed the presence of pancytopenia and hepatosplenomegaly, which led to further workup. The cause was identified as a rare, underrecognized diagnosis of Niemann-Pick disease, a lipid storage disorder. This case elucidates the importance of thoroughly looking into signs and symptoms to reach a diagnosis and the need to recognize inherited metabolic disorders as part of unique clinical presentations, which will lead to overall better patient care and outcomes.
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Registered trials
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