Liddle syndrome misdiagnosed as primary aldosteronism is caused by inaccurate aldosterone-rennin detection while a novel < em > SCNN1G < /em > mutation is discovered

CONCLUSION: inaccurate ARR detection might misdiagnose Liddle syndrome. A Gene test is an important method for the diagnosis of Liddle syndrome. A novel SCNN1G missense mutation, c.1729 C > T, is found in a Chinese family.PMID:35723567 | DOI:10.1080/08037051.2022.2088471

Source: Blood Pressure - June 20, 2022 Category: Hematology Authors: Yaling Yang Chenwei Wu Duoduo Qu Xinyue Xu Lili Chen Quanya Sun Xiaolong Zhao Source Type: research