Evidence map›Paper›PMID 39328859›Full record

ArticleWorld journal of clinical cases2024

HDR syndrome presented with nephrotic syndrome in a Chinese boy: A case report.

Li-Juan Ma, Wu Yang, Hong-Wen Zhang

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in World journal of clinical cases, 2024. 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
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.

  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

3 authors.

Li-Juan MaDepartment of Pediatrics, Peking University First Hospital Ningxia Women and Children's Hospital, Yinchuan 750001, Ningxia Hui Autonomous Region, China.
Wu YangDepartment of Pediatrics, Peking University First Hospital Ningxia Women and Children's Hospital, Yinchuan 750001, Ningxia Hui Autonomous Region, China.
Hong-Wen ZhangDepartment of Pediatrics, Peking University First Hospital Ningxia Women and Children's Hospital, Yinchuan 750001, Ningxia Hui Autonomous Region, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHDR syndrome is a rare genetic disease caused by variants in the CASE SUMMARY: A 9-month-old boy was hospitalized with a complaint of diarrhea. Proteinuria was detected in the patient by routine testing for 3 days. No edema, oliguria, fever or abnormal urine color were observed. Routine urinary tests at a local hospital revealed proteinuria (protein 3 +) and microscopic hematuria (red blood cells 5-10/HP). The patient was born by cesarean delivery due to placental abruption at 35 weeks + 4 days of gestation. Intrauterine growth retardation was detected beginning at 6 months of gestation. His birth weight was 1.47 kg (< P3

conclusionWe report an infant with HDR syndrome who presented with early-onset nephrotic syndrome in China. We suggest that variants in the

Indexed as

Case reportChinaHDR syndromeNephrotic syndromeSensorineural deafness

Identifiers

PMID39328859
PMCPMC11326111

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.