@inbook{b99975d921f2452f83489a68880103ca,
title = "Multiple endocrine neoplasia type 1: Clinical manifestations and management",
abstract = "Multiple endocrine neoplasia type I (MEN-1) is an autosomal dominant syndrome associated with anterior pituitary, parathyroid, and enteropancreatic endocrine tumors as well as other endocrine and nonendocrine tumors [1]. MEN-1 is defined as the presence of two of three main MEN-1-related manifestations, or at least one manifestation plus a first degree relative with at least one MEN-1-related manifestation [1,2]. The estimated prevalence of MEN-1 ranges from 1 in 10,000 to 1 in 100,000 [3], with 43 and 94% penetrance of MEN-1 by ages 20 and 50, respectively [4].",
author = "Powell, {Anathea C.} and Libutti, {Steven K.}",
year = "2010",
doi = "10.1007/978-1-4419-0857-5_16",
language = "English (US)",
isbn = "9781441908568",
series = "Cancer Treatment and Research",
pages = "287--302",
editor = "Cord Sturgeon",
booktitle = "Endocrine Neoplasia",
}
