ArticleCureus2026
Punctate Palmoplantar Keratoderma Type 1 With a Multigenerational Family History: 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.
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Who cites it
0 citing papers in PubMed.
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Punctate palmoplantar keratoderma type 1 (PPKP1), also known as Buschke-Fischer-Brauer disease, is a rare inherited keratinization disorder characterized by multiple hyperkeratotic papules on the palms and soles. It is typically inherited in an autosomal dominant pattern with variable penetrance and has been associated with pathogenic variants in the
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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.