Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a genetic condition where fluid-filled cysts form in the kidneys, leading to kidney enlargement and reduced function over time. It’s inherited from one affected parent, meaning a 50% chance for each child to inherit the disease. Symptoms often include high blood pressure, back pain, and frequent urination. While there’s no cure, management includes monitoring kidney function and treating symptoms. Lifestyle modifications and medications can help slow progression, and in advanced cases, dialysis or kidney transplantation may be necessary. Awareness and early intervention are key to managing ADPKD effectively.