{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,23]],"date-time":"2026-04-23T06:37:02Z","timestamp":1776926222094,"version":"3.51.2"},"reference-count":19,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2026,4,23]],"date-time":"2026-04-23T00:00:00Z","timestamp":1776902400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Pediatr."],"abstract":"<jats:p>Bilateral renal agenesis (BRA) is typically considered a lethal condition due to severe pulmonary hypoplasia caused by early-onset anhydramnios. We report the case of a male infant who survived without prenatal intervention, underwent complex postnatal nephrological and surgical management, and ultimately received a successful renal transplant. 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