Evidence map›Paper›PMID 36540882›Full record

ArticleClinical case reports2022

Novel malformations: Chiari type 1 and hydrocephalus in Zhu-Tokita-Takenouchi-Kim syndrome and novel

Piero Pavone, Federica Saia, Xena Pappalardo, Massimo Barbagallo, Adriana Prato, Renata Rizzo

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

Article in Clinical case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. [Zhu-Tokita-Takenouchi-Kim syndrome in a neonate].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2025
    Article
  3. 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 4 institutions in 1 country.

Piero PavoneUnit of Clinical Pediatrics, AOU "Policlinico", PO "G. Rodolico" University of Catania Catania Italy.
Federica SaiaChild and Adolescent Neurology and Psichiatry, Department of Clinical and Experimental Medicine Catania University Catania Italy.
Xena PappalardoUnit of Catania, Institute for Biomedical Research and Innovation National Council of Research Catania Italy.
Massimo BarbagalloUnit of Pediatrics and Pediatrics Emergency Hospital "G. Garibaldi" Catania Italy.
Adriana PratoChild and Adolescent Neurology and Psichiatry, Department of Clinical and Experimental Medicine Catania University Catania Italy.ORCID https://orcid.org/0000-0003-1083-7915
Renata RizzoChild and Adolescent Neurology and Psichiatry, Department of Clinical and Experimental Medicine Catania University Catania Italy.
University of Catania · ITInstitute for Biomedical Research and Innovation · ITOspedale Garibaldi · ITUniversity of Messina · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zhu-Tokita-Tachenouchi-Kim syndrome (ZTTK) is a recently recognized malformation syndrome presenting with craniofacial dysmorphism, developmental delay/intellectual disability, seizures, anomalies involving brain white matter, and other body-organs. In humans, the disorder is linked to the loss-of-function variants in the

Indexed as

Chiari malformation type 1developmental delayhydrocephalusSON geneZhu‐Tokita‐Tachenouchi‐Kim syndrome (ZTTK)

Identifiers

PMID36540882
PMCPMC9755635
OpenAlexW4311689089

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.