Observational study identifies polyp recurrence variations in pediatric Peutz-Jeghers syndrome, suggesting clinical implications based on STK11 mutation status.
This study reveals distinct clinical profiles across polyp recurrence intervals and between STK11-positive and -negative patients, while delineating the STK11 mutation landscape in pediatric PJS. These findings provide the genomic resource for pediatric PJS, offering critical insights into disease mechanisms and clinical management.
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Yuan et al. (2026) studied this question.
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