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Glucocorticoid‐remediable aldosteronism in a young adult with a family history of Conn's syndrome
Glucocorticoid‐remediable aldosteronism is a hereditary form of primary hyperaldosteronism and the most common monogenic cause of hypertension. We present the case of a 24‐year‐old man with a family history of Conn's syndrome. Yet, in the index patient, classical characteristics of mineralocort...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5799640/ https://www.ncbi.nlm.nih.gov/pubmed/29445488 http://dx.doi.org/10.1002/ccr3.1377 |
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author | Methe, Heiko Pehlivanli, Sinan |
author_facet | Methe, Heiko Pehlivanli, Sinan |
author_sort | Methe, Heiko |
collection | PubMed |
description | Glucocorticoid‐remediable aldosteronism is a hereditary form of primary hyperaldosteronism and the most common monogenic cause of hypertension. We present the case of a 24‐year‐old man with a family history of Conn's syndrome. Yet, in the index patient, classical characteristics of mineralocorticoid excess could be reversed by exogenous glucocorticoids. |
format | Online Article Text |
id | pubmed-5799640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57996402018-02-14 Glucocorticoid‐remediable aldosteronism in a young adult with a family history of Conn's syndrome Methe, Heiko Pehlivanli, Sinan Clin Case Rep Case Reports Glucocorticoid‐remediable aldosteronism is a hereditary form of primary hyperaldosteronism and the most common monogenic cause of hypertension. We present the case of a 24‐year‐old man with a family history of Conn's syndrome. Yet, in the index patient, classical characteristics of mineralocorticoid excess could be reversed by exogenous glucocorticoids. John Wiley and Sons Inc. 2018-01-15 /pmc/articles/PMC5799640/ /pubmed/29445488 http://dx.doi.org/10.1002/ccr3.1377 Text en © 2018 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Methe, Heiko Pehlivanli, Sinan Glucocorticoid‐remediable aldosteronism in a young adult with a family history of Conn's syndrome |
title | Glucocorticoid‐remediable aldosteronism in a young adult with a family history of Conn's syndrome |
title_full | Glucocorticoid‐remediable aldosteronism in a young adult with a family history of Conn's syndrome |
title_fullStr | Glucocorticoid‐remediable aldosteronism in a young adult with a family history of Conn's syndrome |
title_full_unstemmed | Glucocorticoid‐remediable aldosteronism in a young adult with a family history of Conn's syndrome |
title_short | Glucocorticoid‐remediable aldosteronism in a young adult with a family history of Conn's syndrome |
title_sort | glucocorticoid‐remediable aldosteronism in a young adult with a family history of conn's syndrome |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5799640/ https://www.ncbi.nlm.nih.gov/pubmed/29445488 http://dx.doi.org/10.1002/ccr3.1377 |
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