ArticleJournal of neural transmission (Vienna, Austria : 1996)2026
X-linked dystonia parkinsonism as a cause of isolated lingual dystonia (ILD).
Article in Journal of neural transmission (Vienna, Austria : 1996), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Dystonia is a movement disorder characterized by sustained or intermittent muscle contractions that cause abnormal postures or repetitive movements. Isolated lingual dystonia (ILD) is a rare form of oromandibular dystonia, which affects only the tongue and accounts for about 4% of all dystonia cases. This report describes two Filipino males, aged 43 and 48, who developed ILD. The first patient is a 43-year-old male from Cebu, with no significant family history or roots from Panay Island, who was found to carry the X-linked dystonia parkinsonism (XDP)-causing variant highlighting a novel presentation of ILD linked to XDP. The second patient is a 48-year-old male from Roxas City, with a family history suggesting XDP, who presented with ILD initially and later developed tremor, limb dystonia, and bradykinesia. His diagnosis of XDP was confirmed by genetic testing. These cases highlight the importance of considering XDP in the differential diagnosis of ILD among Filipinos, regardless of geographic or familial predispositions. Genetic testing and follow-up examinations are crucial for managing ILD, as it may precede more generalized dystonic and parkinsonian symptoms associated with XDP. This study contributes to the limited literature on ILD and suggests new insights into the clinical variability of XDP.
Indexed as
Identifiers
42606742What OpenQuestion holds
Registered trials
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.