Articles with "max mutation" as a keyword



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Case Report of a Prolactinoma in a Patient With a Novel MAX Mutation and Bilateral Pheochromocytomas

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Published in 2017 at "Journal of the Endocrine Society"

DOI: 10.1210/js.2017-00135

Abstract: Pheochromocytomas are neuroendocrine tumors that can arise sporadically or be inherited as a familial disease, and they may occur in isolation or as part of a multitumor syndrome. Familial disease typically presents in younger patients… read more here.

Keywords: max; prolactinoma; max mutation; bilateral pheochromocytomas ... See more keywords
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Familial Acromegaly and Bilateral Asynchronous Pheochromocytomas in a Female Patient With a MAX Mutation: A Case Report

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Published in 2021 at "Frontiers in Endocrinology"

DOI: 10.3389/fendo.2021.683492

Abstract: Background There are very few cases of co-occurring pituitary adenoma (PA) and pheochromocytomas (PCC)/paragangliomas caused by MAX mutations. No cases of familial PA in patients with MAX mutations have been described to date. Case Presentation… read more here.

Keywords: pcc; case; female patient; max mutation ... See more keywords