MEN1 patients present lactotroph tumors (the most frequent pituitary NETs associated with MEN1, followed by somatotroph tumors) in addition to primary hyperparathyroidism (which typically appears around the age of 20–25 years and is more frequently accompanied by nephrolithiasis than non-MEN hyperparathyroidism) [24,25,26,27,28,29,30]. The gene discussed is MEN1; the disease is primary hyperparathyroidism.