Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Type I Pseudohypoaldosteronism Includes Two Clinically and Genetically Distinct Entities with either Renal or Multiple Target Organ Defects

1 Nov 1991

Abstract excerpt

Type I pseudohypoaldosteronism (PHA) is a hereditary disease characterized by salt wasting resulting from target organ unresponsiveness to mineralocorticoids. We have studied two kindreds including a total of nine patients with PHA. In kindred I, the propositus presented with renal salt wasting in infancy (vomiting, failure to thrive, short stature, hyponatremia, hyperkalemia) and responded dramatically to a high...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cardiovascular, Neuropeptides, and Oxidative Stress Research
Share to Hormonal Regulation and Hypertension
Share to Ion Transport and Channel Regulation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 1939532
DOI: 10.1210/jcem-73-5-936

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Type I Pseudohypoaldosteronism Includes Two Clinically and Genetically Distinct Entities with either Renal or Multiple Target Organ DefectsPMID 1939532Read ↗

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

Mineralocorticoid resistance.Semantic proximity Read ↗

Mechanisms of type I and type II pseudohypoaldosteronism.Semantic proximity Read ↗

Clinical and molecular analysis of six Japanese patients with a renal form of pseudohypoaldosteronism type 1.Semantic proximity Read ↗

Renal pseudohypoaldosteronism type 1 – an adult case series including a novel gene variantSemantic proximity Read ↗

Clinical Manifestations of Pseudohypoaldosteronism with Genotype-phenotype Correlation. A Single Center Experience, A Retrospective Cohort Study.Semantic proximity Read ↗

Clinical and Biochemical Characteristics of Pseudohypoaldosteronism Type 1 with and Without Genetic Mutations: A Literature ReviewSemantic proximity Read ↗

Clinical and molecular features of type 1 pseudohypoaldosteronism.Semantic proximity Read ↗

Inactivating mutations of the mineralocorticoid receptor in Type I pseudohypoaldosteronism.Semantic proximity Read ↗

Pseudohypoaldosteronism Type II: A Young Girl Presented with Hypertension, Hyperkalemia and Metabolic Acidosis.Semantic proximity Read ↗

[Mineralocorticoid resistance: pseudohypoaldosteronism type 1].Semantic proximity Read ↗

Clinical Manifestation and Molecular Analysis of Three Korean Patients with the Renal Form of Pseudohypoaldosteronism Type 1.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.