🧠 Polycystic Kidney Disease (PKD) — Exam Review 1. Types • Autosomal Dominant PKD (ADPKD) → most common (adult onset) • Genes: PKD1, PKD2 mutations • Symptoms appear in 30s–40s • Autosomal Recessive PKD (ARPKD) → rare, severe (childhood onset) 2. Pathophysiology • Cysts form in both kidneys → progressive enlargement → impaired kidney function • Eventually leads to chronic kidney disease (CKD) and ESRD • Also involves extrarenal cysts (liver, pancreas, spleen) 3. Clinical Features • Flank pain,

🚨 Spotlight on Polycystic Kidney Disease (PKD) 🚨 PKD is a genetic disorder that can significantly impact kidney function due to cyst development. Join SciePro as we discuss how this condition progresses, the symptoms to watch for, and the latest treatment strategies. Our goal is to provide support and education to those affected by PKD and raise awareness about kidney health. https://www.sciepro.com/licensing #PKDAwareness #HealthEducation #SciePro #kidney #cyst #disease #meded #anatomy #nephr

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