"Liddle Syndrome" 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.
Familial pseudoaldosteronism characterized by autosomal dominant inheritance of hypertension with HYPOKALEMIA; ALKALOSIS; RENIN and ALDOSTERONE level decreases. It is caused by mutations in EPITHELIAL SODIUM CHANNELS beta and gamma subunits. Different mutations in the same EPITHELIAL SODIUM CHANNELS subunits can cause PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT.
| Descriptor ID |
D056929
|
| MeSH Number(s) |
C12.777.419.815.683 C13.351.968.419.815.683 C16.320.565.861.698 C18.452.648.861.698
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Liddle Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Liddle Syndrome".
This graph shows the total number of publications written about "Liddle Syndrome" by people in this website by year, and whether "Liddle Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2016 | 1 | 0 | 1 |
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Below are the most recent publications written about "Liddle Syndrome" by people in Profiles.
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Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel ?-subunit in a case of early-onset phenotype of Liddle syndrome. Cold Spring Harb Mol Case Stud. 2016 11; 2(6):a001255.