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Liddle syndrome 3

Summary

Liddle syndrome, or pseudoaldosteronism, is an autosomal dominant form of salt-sensitive hypertension characterized by suppressed plasma renin and aldosterone, hypokalemia, and metabolic alkalosis (summary by Salih et al., 2017). For a discussion of genetic heterogeneity of Liddle syndrome, see 177200. [from OMIM]

Available tests

8 tests are in the database for this condition.

Clinical tests (8 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: BESC2, ENaCa, ENaCalpha, LIDLS3, PHA1B1, SCNEA, SCNN1, SCNN1A
    Summary: sodium channel epithelial 1 subunit alpha

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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