📘 Chapter 616.7 · Aldosterone Synthase Deficiency

Nelson Textbook of Pediatrics 22nd Edition | Isolated mineralocorticoid deficiency (salt-wasting, hyperkalemia). CYP11B2 mutations. Normal cortisol, normal ACTH, elevated renin, low aldosterone, elevated 18-hydroxycorticosterone (type II) or low (type I). Treatment: fludrocortisone.

🌐 paeds.online — Pakistan's Pediatric Platform

📋 30 Clinical Scenarios — Aldosterone Synthase Deficiency (FCPS level)

📇 High‑Yield Review Cards: Aldosterone Synthase Deficiency

🩺 Symptom‑Based Approach: Aldosterone Synthase Deficiency

Select a presentation for diagnostic clues.

📋 Stepwise Management of Aldosterone Synthase Deficiency (Nelson Ch 616.7)

⚡ Reflex Prompts — Clinical Decisions in Aldosterone Synthase Deficiency

📖 Summary: Aldosterone Synthase Deficiency — Nelson 22nd Ed