Page last updated: 2024-09-03

chymosin and Liddle Syndrome

chymosin has been researched along with Liddle Syndrome in 1 studies

*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. [MeSH]

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (100.00)2.80

Authors

AuthorsStudies
Chen, L; Qu, D; Sun, Q; Wu, C; Xu, X; Yang, Y; Zhao, X1

Other Studies

1 other study(ies) available for chymosin and Liddle Syndrome

ArticleYear
Liddle syndrome misdiagnosed as primary aldosteronism is caused by inaccurate aldosterone-rennin detection while a novel
    Blood pressure, 2022, Volume: 31, Issue:1

    Topics: Adult; Aldosterone; Chymosin; Diagnostic Errors; Epithelial Sodium Channels; Female; Humans; Hyperaldosteronism; Hypertension; Liddle Syndrome; Mutation; Renin; Young Adult

2022