Evidence map›Paper›PMID 40823463›Full record

ArticleCureus2025

Focal Dystonia in a Patient With Young-Onset Parkinsonism: A Diagnostic Challenge.

Ahmer A Longi, Pushparaja Shetty, Misbah Fazlani, Mohammed Alnims, Nauman Ali

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. 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

5 authors.

Ahmer A LongiInternal Medicine, Mediclinic Welcare Hospital, Dubai, ARE.
Pushparaja ShettyNeurology, Mediclinic Welcare Hospital, Dubai, ARE.
Misbah FazlaniInternal Medicine, Mediclinic Welcare Hospital, Dubai, ARE.
Mohammed AlnimsInternal Medicine, Mediclinic Welcare Hospital, Dubai, ARE.
Nauman AliInternal Medicine, Mediclinic Welcare Hospital, Dubai, ARE.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oropharyngeal dystonia (OPD) is a form of focal dystonia characterized by involuntary movements that affect the facial, labial, and tongue muscles. OPD is frequently underrecognized and underdiagnosed, despite its relatively high prevalence among individuals with Parkinson's disease (PD), including during the early stages of the disease. Limited awareness among both patients and healthcare providers can contribute to delays in diagnosis. We present the case of a 45-year-old Emirati male who presented with left-sided resting tremors followed by progressive tongue dystonia over four months. Clinical and radiological examination revealed him to have early-onset clinically established PD based on the Movement Disorder Society Clinical Diagnostic Criteria 2015. The patient was initiated on dopaminergic therapy, resulting in significant symptom improvement. Early recognition and timely intervention are essential, as they can substantially mitigate morbidity and enhance quality of life. This report examines the characteristics of dystonia, including its prevalence, etiologies, and clinical presentation within the context of early-onset PD, and outlines a tailored strategy to facilitate early diagnosis. The case highlights the importance of recognizing atypical features such as OPD in early-onset PD, which may present diagnostic challenges but respond well to timely treatment.

Indexed as

focal dystoniaoropharyngeal dystoniaparkinsonismtongue dystoniayoung-onset parkinson’s disease

Identifiers

PMID40823463
PMCPMC12357203

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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.