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ARMC5 Primary Bilateral Macronodular Adrenal Hyperplasia Associated with a Meningioma: A Family Report

Primary 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,...

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Detalles Bibliográficos
Autores principales: Ferreira, M. J., Pedro, J., Salazar, D., Costa, C., Aragão Rodrigues, J., Costa, M. M., Grangeia, A., Castedo, J. L., Carvalho, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484682/
https://www.ncbi.nlm.nih.gov/pubmed/32934851
http://dx.doi.org/10.1155/2020/8848151
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author Ferreira, M. J.
Pedro, J.
Salazar, D.
Costa, C.
Aragão Rodrigues, J.
Costa, M. M.
Grangeia, A.
Castedo, J. L.
Carvalho, D.
author_facet Ferreira, M. J.
Pedro, J.
Salazar, D.
Costa, C.
Aragão Rodrigues, J.
Costa, M. M.
Grangeia, A.
Castedo, J. L.
Carvalho, D.
author_sort Ferreira, M. J.
collection PubMed
description Primary 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.
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spelling pubmed-74846822020-09-14 ARMC5 Primary Bilateral Macronodular Adrenal Hyperplasia Associated with a Meningioma: A Family Report Ferreira, M. J. Pedro, J. Salazar, D. Costa, C. Aragão Rodrigues, J. Costa, M. M. Grangeia, A. Castedo, J. L. Carvalho, D. Case Rep Endocrinol Case Report Primary 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. Hindawi 2020-09-02 /pmc/articles/PMC7484682/ /pubmed/32934851 http://dx.doi.org/10.1155/2020/8848151 Text en Copyright © 2020 M. J. Ferreira et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ferreira, M. J.
Pedro, J.
Salazar, D.
Costa, C.
Aragão Rodrigues, J.
Costa, M. M.
Grangeia, A.
Castedo, J. L.
Carvalho, D.
ARMC5 Primary Bilateral Macronodular Adrenal Hyperplasia Associated with a Meningioma: A Family Report
title ARMC5 Primary Bilateral Macronodular Adrenal Hyperplasia Associated with a Meningioma: A Family Report
title_full ARMC5 Primary Bilateral Macronodular Adrenal Hyperplasia Associated with a Meningioma: A Family Report
title_fullStr ARMC5 Primary Bilateral Macronodular Adrenal Hyperplasia Associated with a Meningioma: A Family Report
title_full_unstemmed ARMC5 Primary Bilateral Macronodular Adrenal Hyperplasia Associated with a Meningioma: A Family Report
title_short ARMC5 Primary Bilateral Macronodular Adrenal Hyperplasia Associated with a Meningioma: A Family Report
title_sort armc5 primary bilateral macronodular adrenal hyperplasia associated with a meningioma: a family report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484682/
https://www.ncbi.nlm.nih.gov/pubmed/32934851
http://dx.doi.org/10.1155/2020/8848151
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