Evidence map›Paper›PMID 42569799›Full record

ArticleAutism research : official journal of the International Society for Autism Research2026

Defining and Measuring Developmental Regression During Childhood: A Scoping Review.

Kirsten Furley, Jenny Fairthorne, Vishnu Priya Mohanakumar Sindhu, Katrina Williams, Amanda Brignell

Abstract readScoping Review
In one paragraph

Article in Autism research : official journal of the International Society for Autism Research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Defining and Measuring Developmental Regression During Childhood: A Scoping Review.Autism research : official journal of the International Society for Autism Research · 2026
    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

5 authors.

Kirsten FurleyDepartment of Paediatrics, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0001-6016-2157
Jenny FairthorneDepartment of Paediatrics, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0002-9884-0117
Vishnu Priya Mohanakumar SindhuTurner Institute for Brain and Mental Health, School of Psychological Sciences, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0003-4997-6891
Katrina WilliamsDepartment of Paediatrics, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0001-5096-7752
Amanda BrignellDepartment of Paediatrics, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0003-4324-522X

Funding

Monash University
6 · The paper itself

Abstract

Developmental regression during childhood is inconsistently defined and measured, resulting in delayed diagnostic discovery and intervention. This study aimed to examine published definitions and measures for developmental regression. A comprehensive search strategy was applied to Medline, Embase, Cochrane, and PsycINFO databases. Reviewers independently screened relevant studies according to the Preferred Reporting Items for Systematic reviews. The number and percentages of definition use, their primary features, and measures were reported. Of 19,099 potential publications, 157 were included. Thematic analysis identified four condition groups: Neurodevelopmental disorders (n = 118); Progressive neurodegenerative conditions (n = 17); Developmental epileptic encephalopathies (n = 8); and Genetic conditions (n = 14). Most studies (n = 124, 79.0%) used an operational definition, and most specified types of skills lost (n = 147, 93.6%). Age of onset was specified in 67.5% (n = 106), and duration was specified in 34.4% (n = 54). Measures designed to specifically assess developmental regression were infrequently used (n = 5, 3.2%). We concluded that developmental regression is inconsistently defined and measured. A consistent approach is vital to ensure that all children are identified as early as possible. This will allow timely diagnostic discovery, enhance research rigor, and promote the collaboration that is needed to advance our understanding of causal mechanisms and effective interventions for affected children and their families.

Indexed as

Developmental DisabilitiesNeurodevelopmental DisordersChildHumanschild development disordersdefinitiondevelopmental disabilitiesdevelopmental regressionneurodevelopmental disorderspervasive

Identifiers

PMID42569799
PMCPMC13599686

What OpenQuestion holds

Textmetadata
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.