202 top medical experts on Liddle Syndrome across 21 countries and 7 U.S. states, including 29 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- 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.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Broader Categories (#Experts): Inborn Errors Renal Tubular Transport (984).
- Clinical Trials : at least 1
- Synonyms: Pseudoaldosteronism
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