Multiple Endocrine Neoplasia
Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms
... Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominantly inherited predisposition to neoplastic lesions of the parathyroids, pancreas, and the ...
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Case Report Association between nocardia farcinica opportunistic Infection and type 1 multiple endocrine neoplasia
... Abstract: Background: The global incidence of immunocompromised individuals has increased in recent decades; Many of these individuals are suffering from Nocardiosis. However, this is the first published report of ...
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Diagnosis and Management of Multiple Endocrine Neoplasia Type 1 (MEN1)
... 1. Chandrasekharappa SC, Guru SC, Manickam P, Olufemi SE, Collins FS, Emmert-Buck MR, Debelenko LV, Zhuang Z, Lubensky IA, Liotta LA, Crabtree JS, Wang Y, Roe BA, Weisemann J, Boguski MS, Agarwal SK, Kester MB, Kim YS, ...
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Incidence and prevalence of multiple endocrine neoplasia 2A in Denmark 1901–2014: a nationwide study
... Background: The incidence and prevalence of multiple endocrine neoplasia 2A (MEN2A) have only been reported once in a nationwide setting. However, it is unclear whether the figures are representative ...
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Diagnosis and surgical treatment of multiple endocrine neoplasia type 2A
... Multiple endocrine neoplasia type 2 (MEN 2) is an inherited syndrome which affects many endocrine glands. Generally, MEN 2 is divided into three subtypes: MEN 2A, MEN 2B, and familial ...
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Multiple Endocrine Neoplasia Type 2A in a Kindred With C634Y Mutation
... ABSTRACT. Multiple endocrine neoplasia type 2A (MEN 2A) is most frequently caused by codon 634 acti- vating ...cgi/doi/10.1542/peds.2005-0033; multiple endocrine neo- plasia, MEN 2A, ...
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Multiple endocrine neoplasia type 2
... Multiple Endocrine Neoplasia Type 2 (MEN2) is a rare hereditary complex disorder characterized by the presence of medullary thyroid carcinoma (MTC), unilateral or bilateral pheochromocytoma (PHEO) ...
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Original Article RET gene mutations identified by exome sequencing in a multiple endocrine neoplasia type 2A
... Multiple endocrine neoplasia type 2 (MEN2), also known as the Sipple syndrome, is firstly discovered by Sipple in 1961 [1], which is one autosomal dominant inheritance disease with the incidence rate ...
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Multiple Endocrine Neoplasia Type 1 with Multiple Leiomyomas Linked to a Novel Mutation in the MEN1 Gene
... Multiple endocrine neoplasia type 1 (MEN1) is an auto- somal dominantly inherited ...with multiple leiomyomas in ...with multiple leiomyomas, parathyroid adenoma, pituitary adenoma, ...
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Non functioning Pancreatic Neuroendocrine Tumor in a Patient with Multiple Endocrine Neoplasia Type 1 Syndrome: Case Report
... with Multiple Endocrine Neoplasia Type 1 Syndrome in the same patient, the literature shows 80 to 100% ...three endocrine sites: the parathyroid glands, the pancreatic islet and the Pituitary ...
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A Case of Multiple Endocrine Neoplasia Type 2B and Gangliomatosis of Gastrointestinal Tract
... development in patients affected with RET germ line muta- tions remain unknown. Recent researches suggest that an overrepresentation of mutant RET as a “second hit” event might trigger tumor genesis. However, alterations ...
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Bilateral adrenocortical carcinoma in a patient with multiple endocrine neoplasia type 1 (MEN1) and a novel mutation in the MEN1 gene
... 8. Agarwal SK, Lee Burns A, Sukhodolets KE, Kennedy PA, Obungu VH, Hickman AB, Mullendore ME, Whitten I, Skarulis MC, Simonds WF, Mateo C, Crabtree JS, Scacheri PC, Ji Y, Novotny EA, Garrett-Beal L, Ward JM, Libutti SK, ...
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'Quality in, quality out', a stepwise approach to evidence-based medicine for rare diseases promoted by multiple endocrine neoplasia type 1
... is multiple endocrine neoplasia type 1 (MEN1), which is an autosomal dominant endocrine tumor syndrome with an estimated occurrence rate of 2–3 per ...by multiple endocrine ...
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Concomitant existence of pheochromocytoma in a patient with multiple endocrine neoplasia type 1
... 2. Chandrasekharappa SC, Guru SC, Manickam P, Olufemi SE, Collins FS, Emmert-Buck MR, Debelenko LV, Zhuang Z, Lubensky IA, Liotta LA, Crabtree JS, Wang Y, Roe BA, Weisemann J, Boguski MS, Agarwal SK, Kester MB, Kim YS, ...
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Multiple endocrine neoplasia type 1 presenting with concurrent insulinoma and prolactinoma in early-adolescence
... In pediatrics, hypoglycemia most commonly presents in infants and toddlers. Presentation in early adolescence is unusual, but can be due to ingestions including hypoglycemic agents or ethanol or hormonal causes, such as ...
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Clinical presentation and management of primary ovarian neuroendocrine tumor in multiple endocrine neoplasia type 1
... Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant condition characterized by parathyroid, anterior pituitary and enteropancreatic endocrine cell ...
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Treatment-resistant pediatric giant prolactinoma and multiple endocrine neoplasia type 1
... Background: Pediatric pituitary adenomas are rare, accounting for <3 % of all childhood intracranial tumors, the majority of which are prolactinomas. Consequently, they are often misdiagnosed as other suprasellar ...
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Multiple endocrine neoplasia type 1
... Multiple Endocrine Neoplasia type 1 (MEN1) is a rare autosomal dominant hereditary cancer syndrome presented mostly by tumours of the parathyroids, endocrine pancreas and anterior pituitary, ...
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Fast growing pancreatic neuroendocrine carcinoma in a patient with multiple endocrine neoplasia type 1: a case report
... with multiple endocrine neoplasia type 1 are intended to detect and treat malignant tumors at the earliest stage ...with multiple endocrine neoplasia type 1 are controversial as ...
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Telomere dysfunction suppresses multiple endocrine neoplasia in mice
... 3. Agarwal SK, Kester MB, Debelenko LV, Heppner C, Emmert-Buck MR, Skarulis MC, Doppman JL, Kim YS, Lubensky IA, Zhuang Z, Green JS, Guru SC, Manickam P, Olufemi SE, Liotta LA, Chandrasekharappa SC, et al. Germline ...
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