Conn’s syndrome (unilateral surgically curable adenoma – if it exists) |
Primary adrenocortical hyperplasia [5, 27, 28] |
Familial hyperaldosteronism |
Type I Dexamethasone-suppressible hypertension [30, 33]; chimeric gene causing ACTH-dependent aldosterone production |
Treat with low-dose dexamethasone |
Type II Linked to chromosome 7p22 [29] |
Treat with aldosterone antagonists [34]; rarely surgical |
Gordon’s syndrome [35] |
treat with salt restriction |
Renal tubular sodium channel mutations or alteration |
Liddle’s syndrome [36] and variants [24, 25, 37] |
5-6% of HT in blacks low aldo and renin; treat with amiloride |
Adducin polymorphisms [38] |
Endogenous ouabain [39] |
low aldo and renin; treat with amiloride (possibly rostafuroxin) |
GIP dependent cortisol excess with nodular hyperplasia [40] |