Familial hyperaldosteronism type 1 (Q105935): Difference between revisions
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CID11:ID_1994802431 | |||||||||||||||
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dki-india-ID_1994802431 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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16 August 2026
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Latest revision as of 12:34, 17 August 2026
Type I familial aldosteronism, also called dexamethasone suppressible aldosteronism, is a rare inherited disorder due to the ectopic expression of the aldosterone synthase in the fascicular zone of the adrenal gland and marked with early severe hypertension (often occurring before the age of 20), biological signs of primary aldosteronism of variable intensity, and an abnormal elevated level of 18-oxo- and 18-hydroxycortisol.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1994802431 |
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| English | Familial hyperaldosteronism type 1 |
Type I familial aldosteronism, also called dexamethasone suppressible aldosteronism, is a rare inherited disorder due to the ectopic expression of the aldosterone synthase in the fascicular zone of the adrenal gland and marked with early severe hypertension (often occurring before the age of 20), biological signs of primary aldosteronism of variable intensity, and an abnormal elevated level of 18-oxo- and 18-hydroxycortisol. |
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CID11:ID_1994802431
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dki-india-ID_1994802431
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Concluído
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16 August 2026
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