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Article

Polyuric-polydipsic syndrome in a pediatric case of non-glucocorticoid remediable familial hyperaldosteronism.

Endocrine journal - 1 Jan 2012

Mussa Alessandro, Camilla Roberta, Monticone Silvia, Porta Francesco, Tessaris Daniele, Verna Francesca, Mulatero Paolo, Einaudi Silvia

Abstract excerpt

Familial hyperaldosteronism (FH) encompasses 3 types of autosomal dominant hyperaldosteronisms leading to inheritable hypertension. FH type II (FH-II), undistinguishable from sporadic hyperaldosteronism, represents the most frequent cause of inheritable hypertension and is believed to only manifest in adults. FH-III is a severe variety of PA resistant to pharmacotherapy and recently demonstrated to be caused by...

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Identifiers

PMID: 22447138
DOI: 10.1507/endocrj.ej11-0406

Genes

KCNJ5

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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