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Anorectal malformations (ARM) are a group of rectal and anal birth defects with a European prevalence of about 1 in 2500–5000 live births1–4. These rare and complex conditions require highly specialized reconstructive surgery in early life, often with a temporary defunctioning stoma5–7. ARM are associated with other organ anomalies in 58–78% of patients; therefore, all ARM newborns should be screened for associated anomalies2,5,8–11.
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