Skip to
  1. Homepage
  2. Rare diseases
  3. Search
PrintPrint
Simple search

Simple search

*
(*) mandatory field





Other search option(s)

Hyperaldosteronism, familial, type 2

Orpha number ORPHA404
Prevalence of rare diseases Unknown
Inheritance
  • Autosomal dominant
Age of onset Variable
ICD 10 code
  • E26.0
MIM number
Synonym(s) Adrenal adenoma, familial

Summary

Type 2 familial hyperaldosteronism, inherited as an autosomal dominant trait, causes hypertension secondary to primary aldosteronism that is not suppressed with dexamethasone. Patients present with an adrenal adenoma that secretes aldosterone. The observation of several families affected suggests that the molecular mechanism may be different than in type I familial hyperaldosteronism, but remains to be identified. Diagnostic suspicion should lead to the screening of patients by determining the aldosterone/renin ratio. * Author: Prof. X. Jeunemaitre (Sep. 2000) *

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
Languages :