The cause of familial hyperaldosteronism type 1 is the fusion of two homologous genes on chromosome 8:
The result is a fusion protein with aldosterone synthetase activity which is under the control of corticotropin rather than angiotensin II.
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.