Evidence map›Paper›PMID 36816814›Full record

ArticleCase reports in genetics2023

Manifestations of Intellectual Disability, Dystonia, and Parkinson's Disease in an Adult Patient with

Maria Arvio, Jaana Lähdetie, Hannu Koivu, Antti Sohlberg, Eero Pekkonen

Open access · goldAbstract readCase Reports
In one paragraph

Article in Case reports in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 32% 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, 1 synthesis or guideline pooled it, 1 citations in OpenAlex.

  1. Managing Dystonia in Partington Syndrome.Movement disorders clinical practice · 2026
    Pooled it
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

5 authors at 4 institutions in 1 country.

Maria ArvioWellbeing Service County of Päijät-Häme, Lahti, Finland.ORCID https://orcid.org/0000-0002-2571-7118
Jaana LähdetieDepartment of Child Neurology and General Practice, Turku University and Turku University Central Hospital, Turku, Finland.
Hannu KoivuWellbeing Service County of Päijät-Häme, Lahti, Finland.
Antti SohlbergWellbeing Service County of Päijät-Häme, Lahti, Finland.
Eero PekkonenDepartment of Neurology, Helsinki University Hospital and Department of Clinical Neurosciences (Neurology) University of Helsinki, Helsinki, Finland.ORCID https://orcid.org/0000-0003-1621-8752
Päijät-Hämeen Keskussairaala · FIOulu University Hospital · FITurku University Hospital · FIUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe a 38-year-old male patient with intellectual disability and progressive motor symptoms who lacked an etiological diagnosis for many years. Finally, clinical exome sequencing showed a likely pathogenic variant of the

Identifiers

PMID36816814
PMCPMC9935879
OpenAlexW4319662517

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.