Evidence map›Paper›PMID 42813040›Full record

ArticleNeurology. Genetics2026

Alternating Hemiplegia of Childhood: Development of a Disease-Specific Clinical Rating Scale.

Michela Stagnaro, Carmen Fons, Eleni Panagiotakaki, Alessio Signori, Francesco Danilo Tiziano, Ramona Cordani, Livia Pisciotta, Lino Nobili, Jennifer Anticona, Jaume Campistol Plana and 7 more

Abstract read
In one paragraph

Article in Neurology. Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

17 authors.

Michela StagnaroChild Neuropsychiatry Unit, IRCCS Istituto Giannina Gaslini, Member of the ERN EpiCARE, Genoa, Italy.ORCID https://orcid.org/0000-0002-7041-2858
Carmen FonsDepartment of Pediatric Neurology, Sant Joan de Déu Children's Hospital, Fundació Sant Joan de Déu, Institut de Recerca Sant Joan de Déu, Coordinating Center of the ERN EpiCARE, Barcelona, Spain.ORCID https://orcid.org/0000-0001-7227-1350
Eleni PanagiotakakiDepartment of Pediatric Clinical Epileptology, Sleep Disorders and Functional Neurology in Children, University Hospitals of Lyon (HCL), Member of the European Reference Network (ERN) EpiCARE, France.ORCID https://orcid.org/0000-0003-2611-0227
Alessio SignoriDepartment of Health Sciences, University of Genoa, Italy.ORCID https://orcid.org/0000-0001-6289-9144
Francesco Danilo TizianoSection of Genomic Medicine, Department of Life Sciences and Public Health, Catholic University of Sacred Heart, Rome, Italy.ORCID https://orcid.org/0000-0002-5545-6158
Ramona CordaniChild Neuropsychiatry Unit, IRCCS Istituto Giannina Gaslini, Member of the ERN EpiCARE, Genoa, Italy.ORCID https://orcid.org/0000-0002-7287-4159
Livia PisciottaNeuropsychiatry Unit, ASST Fatebenefratelli Sacco, University of Milan, Italy.ORCID https://orcid.org/0000-0001-7653-981X
Lino NobiliChild Neuropsychiatry Unit, IRCCS Istituto Giannina Gaslini, Member of the ERN EpiCARE, Genoa, Italy.ORCID https://orcid.org/0000-0001-9317-5405
Jennifer AnticonaDepartment of Pediatric Neurology, Sant Joan de Déu Children's Hospital, Fundació Sant Joan de Déu, Institut de Recerca Sant Joan de Déu, Coordinating Center of the ERN EpiCARE, Barcelona, Spain.ORCID https://orcid.org/0000-0001-5854-077X
Jaume Campistol PlanaDepartment of Pediatric Neurology, Sant Joan de Déu Children's Hospital, Fundació Sant Joan de Déu, Institut de Recerca Sant Joan de Déu, Coordinating Center of the ERN EpiCARE, Barcelona, Spain.ORCID https://orcid.org/0009-0009-7531-6249
Maria T PapadopoulouDepartment of Pediatric Clinical Epileptology, Sleep Disorders and Functional Neurology in Children, University Hospitals of Lyon (HCL), Member of the European Reference Network (ERN) EpiCARE, France.ORCID https://orcid.org/0000-0002-2076-5006
Matthildi Athina Papathanasiou TerziDepartment of Pediatric Clinical Epileptology, Sleep Disorders and Functional Neurology in Children, University Hospitals of Lyon (HCL), Member of the European Reference Network (ERN) EpiCARE, France.ORCID https://orcid.org/0000-0002-1964-4813
Alexis A ArzimanoglouDepartment of Pediatric Neurology, Sant Joan de Déu Children's Hospital, Fundació Sant Joan de Déu, Institut de Recerca Sant Joan de Déu, Coordinating Center of the ERN EpiCARE, Barcelona, Spain.ORCID https://orcid.org/0000-0002-7233-2771
Mohamad A MikatiDivision of Pediatric Neurology and Developmental Medicine, Duke University Department of Pediatrics, Durham, NC.ORCID https://orcid.org/0000-0003-0363-8715
Agathe RoubertieService de Neuropédiatrie, CHU Montpellier, Institut des Neurosciences de Montpellier, INSERM U 1298, France; and.ORCID https://orcid.org/0000-0002-8180-4857
Kailash P BhatiaSobell Department of Motor Neuroscience and Movement Disorders, UCL Institute of Neurology, UCL, London, United Kingdom.ORCID https://orcid.org/0000-0001-8185-286X
Elisa De GrandisChild Neuropsychiatry Unit, IRCCS Istituto Giannina Gaslini, Member of the ERN EpiCARE, Genoa, Italy.ORCID https://orcid.org/0000-0002-9733-9216

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objectives: Alternating hemiplegia of childhood (AHC) is a rare neurodevelopmental disorder, primarily caused by pathogenic variants in ATP1A3 that account for approximately 80% of cases. It is characterized by both paroxysmal and chronic neurologic features. Currently, no validated, disease-specific clinical outcome measures exist for AHC, limiting standardized assessment and longitudinal tracking. We aimed to develop and validate the AHC Rating Scale (AHC-RS), a tool applicable across all age groups. We hypothesized that the AHC-RS would demonstrate strong inter-rater reliability and construct validity. Methods: We conducted a multicenter observational study to assess the reliability and validity of the AHC-RS. Patients with clinically or genetically confirmed AHC-the sole inclusion criterion-were recruited from specialized neurology centers in Italy, Spain, and France. Each participant was visited following a standardized video protocol and evaluated independently by 4 trained neurologists using the AHC-RS. The primary outcome was inter-rater reliability, measured using the intraclass correlation coefficient (ICC). Construct validity was assessed through correlation with the Burke-Fahn-Marsden Dystonia Rating Scale. Results: Forty-eight patients, 45.8% men and 54.2% women (median age: 18.6 years - SD: 12.4, range 2-48), were included. The AHC-RS evaluates 4 different domains: Paroxysmal Nonepileptic Manifestations, Epilepsy, Nonparoxysmal Manifestations, and Adaptive Capacities. Inter-rater reliability was excellent across all domains (ICC: 0.95-0.99). Construct validity was supported by a moderate correlation between the AHC-RS total score and the Burke-Fahn-Marsden Scale (Spearman rho = 0.58; 95% CI 0.29-0.78). A strong correlation was observed between the Nonparoxysmal Score and the Adaptive Score ( Discussion: The AHC-RS shows excellent inter-rater reliability and good construct validity, supporting its use as a disease-specific outcome measure for AHC. These findings confirm clinical observations that paroxysmal and chronic symptoms may progress independently and highlight the greater impact of nonparoxysmal features on long-term functional outcomes. This scale offers a standardized tool for both clinical evaluation and future therapeutic trials. Further validation in larger and more diverse cohorts is warranted.

Identifiers

PMID42813040
PMCPMC13621554

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