Liddle syndrome: clinical and cellular abnormalities

Hosp Pract (Off Ed). 1994 Jul 15;29(7):95-8, 104-5. doi: 10.1080/21548331.1994.11443050.

Abstract

Clinical findings resemble those of primary hyperaldosteronism, except that aldosterone secretion is negligible. The fault appears to lie with continuously avid sodium channels in the distal nephron, resulting in excessive salt absorption, potassium wasting, and severe hypertension. Insights gained in this disorder may help clarify more common forms of low-renin hypertension.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adolescent
  • Alkalosis / genetics
  • Alkalosis / metabolism
  • Alkalosis / physiopathology*
  • Female
  • Humans
  • Hypertension / genetics
  • Hypertension / metabolism
  • Hypertension / physiopathology*
  • Hypokalemia / genetics
  • Hypokalemia / metabolism
  • Hypokalemia / physiopathology*
  • Male
  • Pedigree
  • Sodium Channels / physiology
  • Syndrome

Substances

  • Sodium Channels