Panhypopituitarism, characterized by multiple pituitary hormone deficiencies often including growth hormone (GH), thyroid-stimulating hormone (TSH), and adrenocorticotropic hormone (ACTH), has an estimated prevalence between 1 in 16,000 and 1 in 26,000 individuals (1). Here, GH1 is linked to panhypopituitarism.