Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/143560
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dc.creatorFerreira, MJ
dc.creatorPedro, J
dc.creatorSalazar, D
dc.creatorCosta, C
dc.creatorAragão Rodrigues, J
dc.creatorCosta, MM
dc.creatorGrangeia, A
dc.creatorCastedo, JL
dc.creatorCarvalho, D
dc.date.accessioned2022-08-29T14:35:50Z-
dc.date.available2022-08-29T14:35:50Z-
dc.date.issued2020
dc.identifier.issn2090-6501
dc.identifier.urihttps://hdl.handle.net/10216/143560-
dc.description.abstractPrimary bilateral adrenal macronodular hyperplasia is characterized by functioning adrenal macronodules and variable cortisol secretion. Familial clustering suggests a genetic cause that has been confirmed with the identification of some genetic mutations, including inactivating germline mutations, in armadillo repeat containing 5 (ARMC5) gene. The identification of the pathogenic variant enables the physician to identify and treat these patients earlier and more effectively. It has also been noticed that patients with germline causative variants show a different clinical spectrum, presenting specific clinical characteristics, as the association with the presence of meningiomas.
dc.language.isoeng
dc.publisherHindawi
dc.relation.ispartofCase Reports in Endocrinology, vol.2020:8848151
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleARMC5 Primary Bilateral Macronodular Adrenal Hyperplasia Associated with a Meningioma: A Family Report
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.1155/2020/8848151
dc.relation.publisherversionhttps://www.hindawi.com/journals/crie/2020/8848151/
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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