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Glucocorticoid-remediable aldosteronism
rareFamilial hyperaldosteronism type I (FH-I) is a rare heritable, glucocorticoid remediable form of primary aldosteronism (PA) characterized by early-onset hypertension, hyperaldosteronism, variable hypokalemia, low plasma renin activity (PRA), and abnormal production of 18-oxocortisol and 18-hydroxycortisol.
- Identifiers
- MONDO:0007080 OMIM:103900Orphanet:403
- Causal genes
- CYP11B1
- Part of
- Familial hyperaldosteronism
- Also known as
- aldosteronism, glucocorticoid-remediable · dexamethasone sensitive hypertension · dexamethasone-sensitive hypertension · familial hyperaldosteronism type 1 · FH-I
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