MEN type 2 (Sipple syndrome)

MEN type 2, or Sipple syndrome, is a hereditary condition where certain tumors develop in the body, primarily affecting the thyroid, adrenal glands, and other tissues. It often causes medullary thyroid cancer, tumors in the adrenal glands called pheochromocytomas, and growths in the parathyroid glands that regulate calcium. Early detection through genetic testing is important because these tumors can be treated effectively if identified early. The condition is inherited and may require regular monitoring and preventive treatments to manage or reduce health risks associated with these tumors.