Evidence map›Paper›PMID 41705349›Full record

ArticlePrimary health care research & development2026

Experiences of self-identification, diagnosis and support for adults seeking a recognition of tic disorders in the United Kingdom.

Danni Phoenix-Kane, Saskia Keville, E Bethan Davies, Amanda Ludlow

Abstract read
In one paragraph

Article in Primary health care research & development, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Danni Phoenix-Kanehttps://ror.org/0267vjk41University of Hertfordshire, School of Health, Medicine and Life Sciences, UK.ORCID 0000-0002-5343-8458
Saskia Kevillehttps://ror.org/0267vjk41University of Hertfordshire, School of Health, Medicine and Life Sciences, UK.ORCID 0000-0003-2401-5226
E Bethan DaviesUniversity of Nottingham, School of Medicine, UK.ORCID 0000-0003-3134-0879
Amanda Ludlowhttps://ror.org/0267vjk41University of Hertfordshire, School of Health, Medicine and Life Sciences, UK.ORCID 0000-0003-2843-7290

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThis study aimed to examine the experiences of self-identification, diagnosis, and support for adults with tic disorders (including Tourette Syndrome) in the United Kingdom (UK).

backgroundTraditionally viewed as a neurological disorder of childhood-onset, tic disorders have been observed to remit or persist, often in a milder form, into adulthood. However, the reappearance of problematic symptoms after periods of asymptomatic latency might be more common than previously recognized. The medical exposure and standardization of clinical practice for primary adult-onset or non-typical adult-presenting cases of tic disorders is currently limited and poses barriers to diagnosis.

methodsAn online survey of 42 adults with self-identified tic symptomology explored their tic recognition and journey of attaining a confirmed diagnosis and/or self-identifying after the age of 18 in the UK.

findingsNo significant differences were found between adult and childhood-onset cases. Elevated scores on the Acceptance and Action Tic Specific Questionnaire (AAQ-T) correlated with higher overall frequency, intensity, and severity of motor tics from the Adult Tic Questionnaire (ATQ). The AAQ-T was also shown to negatively correlate with increasing age. Nearly all adults expressed dissatisfaction with the diagnostic process, especially regarding information provided and lack of post-diagnostic support. Those who self-identified quoted fear of dismissal, long waiting lists and lack of understanding from clinicians as reasons for not seeking a formal diagnosis. Overall, the results emphasize the importance for a standardized improved comprehension of tic conditions in healthcare including how to best support adults seeking recognition later in life.

Indexed as

Tic DisordersAdolescentAdultFemaleHumansMaleMiddle AgedSurveys and QuestionnairesUnited KingdomYoung Adultadulthooddiagnosisrecognitionself-identificationtic disordertics

Identifiers

PMID41705349
PMCPMC12931986

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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.