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Article

Pseudohypoaldosteronism types I and II: little more than a name in common.

Journal of pediatric endocrinology & metabolism : JPEM - 1 May 2017

Casas-Alba Dídac, Vila Cots Jordi, Monfort Carretero Laura, Martorell Sampol Loreto, Zennaro Maria-Christina, Jeunemaitre Xavier, Camacho Díaz Juan Antonio

Abstract excerpt

Pseudohypoaldosteronism (PHA) comprises a diverse group of rare diseases characterized by sodium and potassium imbalances incorrectly attributed to a defect in aldosterone production. Two different forms of PHA have been described, type I (PHAI) and type II (PHAII). PHAI has been subclassified into renal and systemic. Given the rarity and heterogeneity of this group of disorders we report three patients who carry...

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Identifiers

PMID: 28593901
DOI: 10.1515/jpem-2016-0467

Genes

CUL3

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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Pseudohypoaldosteronism types I and II: little more than a name in common.PMID 28593901Read ↗

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