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Article

Multiple endocrine neoplasia type 1: extensive analysis of a large database of Florentine patients

14 Nov 2018

Abstract excerpt

BACKGROUND: Multiple endocrine neoplasia (MEN1) is a rare inherited multi-tumour syndrome, affecting specific neuroendocrine organs and non-endocrine tissues with a variable spectrum of over 20 possible different combinations, caused by inactivating heterozygote mutations of the MEN1 gene. Disease onset, penetrance, clinical presentation, course and prognosis are all extremely variable, even among individuals...

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PMID: 30428914
DOI: 10.1186/s13023-018-0938-8

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