Evidence map›Paper›PMID 34430961›Full record

ArticleGlobal medical genetics2021

Psychomotor Delay in a Child with

Mahmut C Ergoren, Erdal Eren, Elena Manara, Stefano Paolacci, Pinar Tulay, Sebnem O Sag, Matteo Bertelli, Gamze Mocan, Sehime Gulsun Temel

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Global medical genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Mahmut C ErgorenDepartment of Medical Genetics, Faculty of Medicine, Near East University, Nicosia, Cyprus.
Erdal ErenDepartment of Pediatric Endocrinology, Faculty of Medicine, Bursa Uludağ University, Bursa, Turkey.
Elena ManaraMAGI's LAB S.r.l., Rovereto, Italy.
Stefano PaolacciMAGI's LAB S.r.l., Rovereto, Italy.
Pinar TulayDepartment of Medical Genetics, Faculty of Medicine, Near East University, Nicosia, Cyprus.
Sebnem O SagDepartment of Medical Genetics, Faculty of Medicine, Bursa Uludag University, Bursa, Turkey.
Matteo BertelliMAGI's LAB S.r.l., Rovereto, Italy.
Gamze MocanDepartment of Medical Genetics, Faculty of Medicine, Near East University, Nicosia, Cyprus.
Sehime Gulsun TemelDepartment of Medical Genetics, Faculty of Medicine, Bursa Uludag University, Bursa, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Achondroplasia (ACH) is a hereditary disorder of dwarfism that is caused by the aberrant proliferation and differentiation of chondrocyte growth plates. The common findings of macrocephaly and facial anomalies accompany dwarfism in these patients.

Indexed as

achondroplasiaFGFR3 mutationspsychomotor delay

Identifiers

PMID34430961
PMCPMC8378917

What OpenQuestion holds

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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.