ReviewJournal of racial and ethnic health disparities2026
Early-Onset Colorectal Cancer in Neglected Populations: Would South Africa's Strategies Improve Screening, Management, and Genetic Insights Worldwide?
Review in Journal of racial and ethnic health disparities, 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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Authors and funding
3 authors.
Funding
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Abstract
Hereditary colorectal cancer (CRC) is recognized as an escalating global public health concern, yet it remains neglected among ethnic minority, indigenous, and/or understudied populations. This study aimed to evaluate the current genetic and molecular research on hereditary and early-onset CRC in these neglected groups. A comprehensive review of literature published from 2018 to 2024 was conducted to characterize the profiles of CRC screening, diagnosis, and management in diverse underserved populations worldwide. The findings indicated that although the molecular features associated with Lynch syndrome were largely consistent across different groups, significant discrepancies were observed in early-onset CRC presentations when compared with well-studied populations. These observations suggested that neglected populations harbored unique genetic profiles that could advance the understanding of CRC pathogenesis and inform broader genetic research on other hereditary disorders. Furthermore, the feasibility of implementing the strategies developed for indigenous South African populations on a global scale was critically assessed. It was concluded that unified, region-specific approaches were essential to enhance early diagnosis, improve interventions, and ultimately contribute to a more equitable global health landscape in the management of hereditary CRC.
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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.