MeSH 搜索器

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.
推出的年份: 2010
副标题
树号: C12.050.351.968.419.815.683, C12.200.777.419.815.683, C12.950.419.815.683, C16.320.831.698
MeSH 单一 ID: D056929
进入的组:
  • Syndrome, Liddle
  • Pseudoaldosteronism

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