Glucocorticoid-remediable aldosteronism in a young adult with a family history of Conn's syndrome.

Clin Case Rep

Department of Cardiology Kliniken an der Paar Krankenhaus Aichach Aichach Germany.

Published: February 2018

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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5799640PMC
http://dx.doi.org/10.1002/ccr3.1377DOI Listing

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  • Primary aldosteronism (PA) is a significant cause of hypertension, and familial hyperaldosteronism type 1 (FH-1) is a hereditary form that can lead to severe health issues, making early detection important.
  • A study analyzed genetic testing data for FH-1 in New Zealand from April 2010 to October 2023, revealing that only 147 tests were conducted, with a positive result in 12.9% of cases and significant variations in testing rates by region.
  • Although testing rates for FH-1 have increased over the years, they are still considered low, indicating a need for more awareness and testing, especially for individuals diagnosed with PA at a young age or those with a family
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