Evidence map›Paper›PMID 37020656›Full record

ArticleFrontiers in pediatrics2023

Case report: Two cases of Poirier-Bienvenu neurodevelopmental syndrome and review of literature.

Xiaolan Chen, Yunli Han, Xing Li, Shiqin Huang, Hai Yuan, Yuanhan Qin

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Comprehensive analysis ofmedRxiv : the preprint server for health sciences · 2026
    Article
  3. CSNK2B Mutation: A Rare Cause of IGHD.Clinical endocrinology · 2025
    Article
  4. 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

6 authors at 2 institutions in 1 country.

Xiaolan ChenDepartment of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Yunli HanDepartment of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Xing LiDepartment of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Shiqin HuangDepartment of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Hai YuanDepartment of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Yuanhan QinDepartment of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
First Affiliated Hospital of GuangXi Medical University · CNGuangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Poirier-Bienvenu neurodevelopmental syndrome (POBINDS) is a rare disease caused by mutations in the CSNK2B gene, which is characterized by intellectual disability and early-onset epilepsy. Mosaicism has not been previously reported in CSNK2B gene. POBINDS is autosomal dominant and almost all reported cases were

Indexed as

CSNK2B genedevelopmental delayMOSAICPoirier-Bienvenu neurodevelopmental syndrome (POBINDS)seizurevariant

Identifiers

PMID37020656
PMCPMC10067874
OpenAlexW4327977382

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.