This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Familial hyperaldosteronism type 1

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

This is a rare cause of autosomal dominant, glucocorticoid-remediable hyperaldosteronism.

Patients suffer from variable severity of:

  • hypertension
  • hypokalaemia

Males are typically more severely affected than females.


Related pages

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.