Liddle Syndrome
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.
Year introduced: 2010
PubMed search builder options
Subheadings:
Tree Number(s): C12.050.351.968.419.815.683, C12.200.777.419.815.683, C12.950.419.815.683, C16.320.831.698
MeSH Unique ID: D056929
Entry Terms:
- Syndrome, Liddle
- Pseudoaldosteronism
See Also: