PMID- 15719382 OWN - NLM STAT- MEDLINE DCOM- 20050325 LR - 20161124 IS - 0022-4790 (Print) IS - 0022-4790 (Linking) VI - 89 IP - 3 DP - 2005 Mar 1 TI - Multiple endocrine neoplasia type 1. PG - 143-50 AB - Multiple endocrine neoplasia-1 (MEN-1) is an autosomal dominant inherited syndrome that occurs due to inactivating mutations of the MEN1 gene locus, coding for a tumor-suppressor protein, menin. The components of MEN-1 are hyperparathyroidism due to multiple parathyroid adenomas, pancreatic neuroendocrine tumors, and pituitary adenomas, in addition to some less common neoplastic manifestations. Care of people with MEN-1 requires knowledge of the problems that may arise, and the best approaches to detect and care for the manifestations of this incurable, but manageable, disease. CI - (c) 2005 Wiley-Liss, Inc. FAU - Doherty, Gerard M AU - Doherty GM AD - NW Thompson Professor of Surgery, University of Michigan, Ann Arbor, Michigan, USA. gerardd@umich.edu LA - eng PT - Journal Article PT - Review PL - United States TA - J Surg Oncol JT - Journal of surgical oncology JID - 0222643 RN - 0 (MEN1 protein, human) RN - 0 (Proto-Oncogene Proteins) SB - IM MH - Adenoma/diagnosis MH - Endosonography MH - Female MH - *Genes, Tumor Suppressor MH - Humans MH - Hyperparathyroidism/etiology MH - Insulinoma/diagnostic imaging/surgery MH - Male MH - *Multiple Endocrine Neoplasia Type 1/diagnosis/genetics/surgery MH - Neuroectodermal Tumors/diagnostic imaging MH - Pancreatic Neoplasms/diagnostic imaging/surgery MH - Parathyroid Neoplasms/diagnosis MH - Pituitary Neoplasms/surgery MH - Prolactinoma/surgery MH - Proto-Oncogene Proteins/*genetics MH - Tomography, Emission-Computed, Single-Photon MH - Tomography, X-Ray Computed MH - Vipoma/surgery RF - 35 EDAT- 2005/02/19 09:00 MHDA- 2005/03/26 09:00 CRDT- 2005/02/19 09:00 PHST- 2005/02/19 09:00 [pubmed] PHST- 2005/03/26 09:00 [medline] PHST- 2005/02/19 09:00 [entrez] AID - 10.1002/jso.20181 [doi] PST - ppublish SO - J Surg Oncol. 2005 Mar 1;89(3):143-50. doi: 10.1002/jso.20181.