Kyuma M, Ura N, Torii T, Takeuchi H, Takizawa H, Kitamura K, Tomita K, Sasaki S, Shimamoto K
The Second Department of Internal Medicine, Sapporo Medical University School of Medicine, Japan.
Clin Exp Hypertens. 2001 Aug;23(6):471-8. doi: 10.1081/ceh-100104238.
Liddle's syndrome is a rare form of autosomal-dominant salt-sensitive hypertension. Constitutive activation of the amiloride-sensitive distal renal epithelial sodium channel (ENaC) is essential for salt-sensitive hypertension. Recently, several DNA analysis studies have indicated that there is a mutation of C-terminus of either the beta or y subunit. We sequenced the C-termini of the beta and -gamma subunits of the ENaC in a Japanese family with hypertension and hypopotassemia without excess minerarocorticoids, clinically diagnosed as Liddle's syndrome. The mutation of the ENaC of this family was beta R564X. Since such case seem to be rare in the literature, detailed data are shown in this report.
利德尔综合征是一种罕见的常染色体显性盐敏感性高血压。氨氯地平敏感的远端肾上皮钠通道(ENaC)的组成性激活是盐敏感性高血压的关键。最近,多项DNA分析研究表明,β或γ亚基的C末端存在突变。我们对一个临床诊断为利德尔综合征的日本高血压和低钾血症家族进行了ENaCβ和γ亚基C末端测序,该家族无盐皮质激素过多情况。该家族ENaC的突变是βR564X。鉴于此类病例在文献中似乎罕见,本报告展示了详细数据。