Evidence map›Paper›PMID 37091313›Full record

ArticleGlobal medical genetics2023

NGS-Panel Diagnosis Developed for the Differential Diagnosis of Idiopathic Toe Walking and Its Application for the Investigation of Possible Genetic Causes for the Gait Anomaly.

David Pomarino, Anna Emelina, Jens Heidrich, Kevin Rostásy, Svenja Schirmer, Jan O Schönfeldt, Anneke Thren, Ferdinand Wagner, Johanna Ronja Thren, Nina Berger

Open access · diamondAbstract read
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Article in Global medical genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 6 citations in OpenAlex.

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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

10 authors at 6 institutions in 2 countries.

David PomarinoPraxis Pomarino, Hamburg, Germany.
Anna EmelinaPraxis Pomarino, Hamburg, Germany.
Jens HeidrichLabor Dr. Heidrich und Kollegen MVZ GmbH, Hamburg, Germany.
Kevin RostásyKinderklinik Datteln, Datteln, Germany.
Svenja SchirmerSANA Klinikum Offenbach, Offenbach, Germany.
Jan O SchönfeldtInstitut für Kinderneurologie, Hamburg, Germany.
Anneke ThrenKinderorthopädie am Pferdeturm, Hanover, Germany.
Ferdinand WagnerDepartment of Orthopedics and Trauma Surgery, Musculoskeletal University Center Munich, University Hospital, Ludwig-Maximilians-University, Munich, Germany.
Johanna Ronja ThrenAnthropology Department, Durham University, Durham, United Kingdom.
Nina BergerInstitut für Kinderneurologie, Hamburg, Germany.
HNO-Praxis · DEDurham University · GBLudwig-Maximilians-Universität München · DEMedizinisches Versorgungszentrum Prof. Mathey, Prof. Schofer · DESana Klinikum Offenbach · DEVestische Caritas-Kliniken · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic toe walking (ITW) describes a condition affecting approximately 4.5% of children. Toe walking is an accompanying symptom for many hereditary disorders. This retrospective study uses next-generation sequencing-panel-diagnosis to investigate the feasibility of genetic testing to research the possible genetic causes of ITW and for differential diagnosis. Data were taken from our inhouse database, the minimum age for participants was 3 years. Underlying neurological or orthopaedic conditions were tested for and ruled out prior to diagnosing ITW. Patients, who experienced complications before, during or immediately after birth, children with autism, and patients toe walking less than 50% of the time were excluded. Eighty-nine patients were included in the study, in which 66 (74.2%) patients were boys and 23 (25.8%) girls. Mean age at testing was 7.7 years (range: 3-17 years). Fifteen of the 89 patients included in the study (16.9%) had a genetic variant identified as likely pathogenic or pathogenic by the genetics laboratory. Additionally, we found 129 variants of uncertain significance. About 65.2% of patients showed a pes cavus foot deformity, 27% of patients reportedly had at least one relative who also displayed the gait anomaly, and 37.1% had problems with their speech development. Despite the limitations of the sample size and the scope of our genetic testing targets, our results indicate that research into the genetic causes of ITW could better our understanding of the causes of ITW in otherwise healthy children, to help develop novel methods to detect serious conditions early. ITW could be an early onset symptom for further hereditary conditions.

Indexed as

cause toe walkingidiopathic toe walkingITWpes cavustoe walking family history

Identifiers

PMID37091313
PMCPMC10121371
OpenAlexW4366725727

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Registered trials

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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.