Evidence map›Paper›PMID 41377777›Full record

ArticleEuropean journal of case reports in internal medicine2025

Pseudohypoaldosteronism type II: The Relevance of A Challenging Diagnosis.

Daniela Cruz, Inês Pintassilgo

Abstract read
In one paragraph

Article in European journal of case reports in internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Daniela CruzInternal Medicine, Hospital Garcia da Orta, Almada, Portugal.
Inês PintassilgoInternal Medicine, Hospital Garcia da Orta, Almada, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pseudohypoaldosteronism type II (PHA II) is a rare genetic syndrome caused by mutations in the LEARNING POINTS: We report a case of a young woman with PHA II caused by a novel variant in

Indexed as

Gordon syndromehyperkalaemiaKLHL3 genelow renin hypertensionPseudohypoaldosteronism type II

Identifiers

PMID41377777
PMCPMC12688584

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.