🧬 Chapter 574 · Congenital Anomalies and Dysgenesis of the Kidneys

Nelson Textbook of Pediatrics 22nd Edition | Renal agenesis, dysplasia, multicystic dysplastic kidney (MCDK), hypoplasia, horseshoe kidney, renal cysts, and associated syndromes. Embryology, clinical presentation, imaging, management, and long-term outcomes.

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πŸ“‹ 30 Clinical Scenarios β€” Congenital Anomalies & Dysgenesis of the Kidneys

πŸ“‡ High‑Yield Review Cards (Kidney Dysgenesis)

🩺 Clinical Recognition: Renal Anomalies & Dysgenesis

Select a presentation for diagnostic clues and management.

πŸ“‹ Stepwise Approach to Congenital Kidney Anomalies

πŸ”‘ Key Principles β€” Nelson Ch 574
β€’ Renal agenesis: Unilateral (1/450-1000 births) often associated with VACTERL, MRKH, Zinner syndrome. Contralateral hypertrophy.
β€’ MCDK: Most common abdominal mass in newborn; cysts regress by age 7; risk of HTN (0.2-1.2%) and Wilms tumor (~1/1200).
β€’ Horseshoe kidney: 1/400-500, higher risk of UPJ obstruction, stones, Wilms tumor (4x).
β€’ Renal dysplasia/hypoplasia: Abnormal metanephric differentiation; oligomeganephronia β†’ ESRD.
β€’ Follow-up solitary kidney: Periodic BP, urinalysis, avoid contact sports? AAP allows sports, counsel about injury risk.

    ⚑ Reflex Prompts β€” Clinical Decisions in Renal Dysgenesis

    πŸ“– Summary: Congenital Anomalies & Dysgenesis of Kidneys β€” Nelson Ch 574