Evidence map›Paper›PMID 34622611›Full record

ArticleSichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition2021

[A Case of Pseudohypoaldosteronism Type Ⅱ (PHA2) Caused by a Novel Mutation of

Wei-Wei Tang, Wan-Xia Ma, Shi-Yi Sun, Xing-Wu Ran

Open access · greenAbstract readCase Reports
In one paragraph

Article in Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 80% of its field
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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. 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

4 authors at 1 institution in 1 country.

Wei-Wei TangDiabetic Foot Care Centre, Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu 610041, China.
Wan-Xia MaDiabetic Foot Care Centre, Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu 610041, China.
Shi-Yi SunDiabetic Foot Care Centre, Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu 610041, China.
Xing-Wu RanDiabetic Foot Care Centre, Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu 610041, China.
Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The patient, a 41-year-old woman, was admitted because "it was found out she had elevated serum potassium levels for 18 days". Eighteen days prior to admission at our hospital, the patient was found to have elevated serum potassium during hospitalization at another hospital, where the patient received symptomatic treatment and was discharged after her serum potassium returned to a normal level. However, the patient still had elevated serum potassium repeatedly and was referred to our hospital for further examination. The patient had a history of acute nephritis and gestational hypertension. Six months prior to admission at our hospital, it was found out that the patient had slightly elevated blood pressure, but no intervention was done. The patient's father has a history of hypertension and diabetes. After admission, laboratory results showed that the patient had hyperkalemia, hyperchloremia and metabolic acidosis. The level of plasma renin was obviously below the normal range, but the concentration of plasma aldosterone was within the normal range. A new mutation locus (c.1115delG) in

Indexed as

HypertensionPseudohypoaldosteronismAdaptor Proteins, Signal TransducingAdultAldosteroneFemaleHumansMicrofilament ProteinsMutationPotassiumAdaptor Proteins, Signal TransducingAldosteroneKLHL3 protein, humanMicrofilament ProteinsPotassiumGene mutationGordon syndromeHydrochlorothiazide hydrochlorideHyperkalemiaMetabolic acidosisPseudohypoaldosteronism type ⅡSingle gene inheritance disease

Identifiers

PMID34622611
PMCPMC10408889
OpenAlexW3204706452

What OpenQuestion holds

Textmetadata
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.