Familial hyperaldosteronism type 1 (Q105935): Difference between revisions
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O hiperaldosteronismo familiar tipo I, também chamado de aldosteronismo supressível por dexametasona, é uma doença hereditária rara devido à expressão ectópica da aldosterona sintase na zona fascicular da glândula adrenal e marcada com hipertensão grave precoce (frequentemente ocorrendo antes dos 20 anos), sinais biológicos de aldosteronismo primário de intensidade variável e um nível elevado anormal de 18-oxo e 18-hidroxicortisol. | |||||||||||||||
| description / en | description / en | ||||||||||||||
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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| Property / Canonical URI: https://id.who.int/icd/entity/1994802431 / rank | |||||||||||||||
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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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| Property / Collection date: 16 August 2026 / rank | |||||||||||||||
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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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