Multiple endocrine neoplasia type 1: Revision history

Diff selection: Mark the radio buttons of the revisions to compare and hit enter or the button at the bottom.
Legend: (cur) = difference with latest revision, (prev) = difference with preceding revision, m = minor edit.

30 April 2024

  • curprev 11:4711:47, 30 April 2024‎ Ai talk contribs‎ 3,862 bytes +3,862‎ Created page with "== Overview == Multiple endocrine neoplasia type 1 (MEN1) is a rare hereditary disorder that primarily affects the endocrine glands. It is characterized by the development of tumors in the parathyroid, pituitary, and pancreatic islet cells. The condition is caused by mutations in the MEN1 gene, which provides instructions for producing a protein that acts as a tumor suppressor. Image:Detail-75761.jpg|thumb|center|A close-up image..."
Retrieved from "https://canonica.ai/page/Multiple_endocrine_neoplasia_type_1"