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Primary hyperparathyroidism in multiple endocrine neoplasia type 1: when to perform surgery?
Clinics, 2012 Primary hyperparathyroidism is a common endocrinological disorder. In rare circumstances, it is associated with familial syndromes, such as multiple endocrine neoplasia type 1.
Francesco Tonelli +2 more
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Multiple endocrine neoplasia type 1
Expert Review of Endocrinology & Metabolism, 2009Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal-dominant inherited tumor syndrome characterized by hyperplasia and/or tumors in the parathyroid glands, the pancreatic islets, the anterior pituitary and adrenal glands, as well as neuroendocrine tumors in the thymus, lungs and stomach, and tumors in nonendocrine tissues.
Cornelis Jm, Lips +3 more
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Multiple endocrine neoplasia type 1
European Journal of Internal Medicine, 2008The co-occurrence of parathyroid hyperplasia with pancreatic endocrine tumours and/or pituitary adenoma is classified as Multiple Endocrine Neoplasia type 1 (MEN-1) and is caused by a germ-line mutation in MEN-1 gene encoding a tumour suppressor protein, menin.
Grzegorz, Piecha +2 more
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Multiple endocrine neoplasia type 1
Clinics in Endocrinology and Metabolism, 1980Multiple endocrine neoplasia (MEN) syndromes are familial disorders inherited as autosomal dominant traits , in which tumours or hyperplasia occur in two or more endocrine organs. MEN is divided into two types, Wenner's syndrome (type I) and Sipple's syndrome (type 2). The difference between the two types lies in the endocrine organs affected.
K, Yamaguchi, T, Kameya, K, Abe
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Multiple endocrine neoplasia type 1 with pyonephrosis
International Journal of Urology, 2002AbstractA case of multiple endocrine neoplasia type 1 (MEN 1) with a clinical manifestation of pyonephrosis is reported. A 47‐year‐old woman with a 14‐year history of renal stones was initially seen with pyonephrosis. The patient was found to have elevated serum levels of parathyroid hormone and growth hormone.
Akinori, Satoh, Tomohiko, Iigaya
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A family with Multiple Endocrine Neoplasia Type 1
Irish Journal of Medical Science, 1983A family of 4 siblings is described in which 3 sisters have Multiple Endocrine Neoplasia Type I (Wermer's Syndrome). All 3 have had Zollinger-Ellison syndrome. One sister in addition had pituitary and parathyroid adenomata, while a second had hyperparathyroidism. It is possible that their father had Zollinger-Ellison syndrome.
M R, Lucey, S, McCann, D G, Weir
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Multiple endocrine neoplasia type 1: a chromatin writer’s block
Journal of Internal Medicine, 2009Abstract.Multiple endocrine neoplasia type 1 (MEN1) is caused by inactivating germ line mutations of the MEN1 tumour suppressor gene. The MEN1 gene product, menin, participates in many cellular processes, including regulation of gene transcription. As part of a protein complex that writes a trimethyl mark on lysine 4 of histone H3 (H3K4me3), menin is ...
Dreijerink, K. M A +2 more
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Multiple Endocrine Neoplasia: Types 1 and 2
2011Multiple endocrine neoplasia type 1 (MEN 1) and type 2 (MEN 2) are autosomal-dominantly inherited syndromes where highly penetrant germline mutations predispose patients to the development of tumours in hormone-secreting cells. In the case of MEN 1, loss-of-function germline mutations in the tumour suppressor gene MEN1 increase the risk of developing ...
Deborah J, Marsh, Oliver, Gimm
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Pancreatic Neuroendocrine Neoplasms in Multiple Endocrine Neoplasia Type 1
International Journal of Molecular Sciences, 2021Francesco Tonelli +2 more
exaly