"Hypoaldosteronism" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A congenital or acquired condition of insufficient production of ALDOSTERONE by the ADRENAL CORTEX leading to diminished aldosterone-mediated synthesis of Na(+)-K(+)-EXCHANGING ATPASE in renal tubular cells. Clinical symptoms include HYPERKALEMIA, sodium-wasting, HYPOTENSION, and sometimes metabolic ACIDOSIS.
| Descriptor ID |
D006994
|
| MeSH Number(s) |
C19.053.500.480
|
| Concept/Terms |
Hypoaldosteronism, Hyporeninemic- Hypoaldosteronism, Hyporeninemic
- Type IV Renal Tubular Acidosis
- Renal Tubular Acidosis, Type IV
- Acidosis, Renal Tubular Type IV
- Hyporeninemic Hypoaldosteronism
|
Below are MeSH descriptors whose meaning is more general than "Hypoaldosteronism".
Below are MeSH descriptors whose meaning is more specific than "Hypoaldosteronism".
This graph shows the total number of publications written about "Hypoaldosteronism" by people in this website by year, and whether "Hypoaldosteronism" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hypoaldosteronism" by people in Profiles.
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Considering Postoperative Functional Hypoaldosteronism after Unilateral Adrenalectomy. Am Surg. 2017 Jun 01; 83(6):598-604.
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Congenital hyperreninemic hypoaldosteronism unlinked to the aldosterone synthase (CYP11B2) gene. J Clin Endocrinol Metab. 2001 Nov; 86(11):5379-82.