Autosomal dominant PKD (Polycystic Kidney Disease) is a genetic disorder characterized by the formation of numerous cysts in the kidneys. These cysts can lead to kidney enlargement and may impair kidney function over time. The condition is caused by mutations in specific genes, primarily PKD1 and PKD2, which are inherited in an autosomal dominant pattern, meaning only one copy of the mutated gene from an affected parent can cause the disease in their offspring. Symptoms of autosomal dominant PKD often appear in adulthood and may include high blood pressure, back or side pain, and frequent urinary tract infections. While there is no cure, management focuses on controlling symptoms and preventing complications. Regular monitoring and lifestyle changes can help maintain kidney health and overall well-being for those affected by this condition.