Multiple endocrine neoplasia type 4

Multiple endocrine neoplasia type 4 (MEN4) is a very rare form of MEN, an inherited cancer syndrome, characterized by parathyroid and anterior pituitary tumors, possibly associated with adrenal, renal, and reproductive organ tumors.

Also known as: CDKN1B multiple endocrine neoplasia, MEN4, multiple endocrine neoplasia caused by mutation in CDKN1B, multiple endocrine neoplasia type 4, multiple endocrine neoplasia, type IV, multiple endocrine neoplasia, type 4

32 clinical trials for this condition and its sub-types, 0 tagged with Multiple endocrine neoplasia type 4 itself.