ASCP Pathology Assistant Practice Exam

Autosomal Dominant Polycystic Kidney Disease (ADPKD) is typically diagnosed in adults, particularly in the age group of around 15-30 years. While the genetic mutation responsible for ADPKD can be present from birth, the manifestations of the disease and the development of symptoms often do not appear until later in life. Early signs may be subtle or even absent during childhood and adolescence, making it less common for the disease to be diagnosed in those younger than 15.

In adults, the condition may present with hypertension, abdominal or flank pain, or complications related to kidney function decline, prompting further investigation and diagnosis. This timing aligns with the typical age of diagnosis for this condition, as individuals begin to experience complications and seek medical attention.