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PedAM

Pediatric Disease Annotations & Medicines




Disease tremor
Phenotype C0013421|dystonia
Sentences 17
PubMedID- 23243072 Results: tdt was higher in patients who had tremor associated with dystonia than in those with essential tremor and healthy controls (110.6 +/- 31.3 vs 63.1 +/- 15.2 vs 62.4 +/- 9.2; p < 0.001).
PubMedID- 25957637 Their phenotypes range from pure cervical dystonia associated with hand tremor to truncal and more generalized dystonic postures.
PubMedID- 24092288 Isolated dystonia (with dystonic tremor) can be caused by mutations in tor1a (dyt1), tubb4 (dyt4), thap1 (dyt6), prkra (dyt16), ciz1 (dyt23), ano3 (dyt24), and gnal (dyt25).
PubMedID- 24744729 Differences in gender, body distribution and temporal thresholds of tremor between patients with dystonia and tremor and those of patients with essential tremor also indicate that tremor in dystonia and essential tremor are different entities (defazio et al., 2013; tinazzi et al., 2013).
PubMedID- 23814537 Both forms of tremor in dystonia frequently resemble essential tremor or another pure tremor syndrome (e.g., isolated head and voice tremors and task-specific writing tremor), and relationships among these tremor disorders have long been debated.
PubMedID- 24137554 A negative dat-spect can support a variety of diagnoses in the right clinical context, including psychogenic parkinsonism, dopa-responsive dystonia associated with parkinsonism, essential tremor, vascular parkinsonism, or drug-induced parkinsonism.
PubMedID- 25663232 Is tremor in dystonia a phenotypic feature of dystonia.
PubMedID- 24442708 In summary, ano3 causes a varied phenotype of young-onset or adult-onset craniocervical dystonia with tremor and/or myoclonic jerks.
PubMedID- 20670416 The coexistence of postural and/or kinetic tremor with dystonia is relatively common and is present in 4-55% patients with focal dystonia [8,13,14].
PubMedID- 24468074 He developed cervical dystonia with dystonic tremor at age 32 years and has benefited from onabotulinumtoxina injections since 38 years of age.
PubMedID- 23757263 A missense mutation in this gene was published as the likely cause of focal, adult-onset cervical dystonia, variably associated with mild tremor, which was inherited as an autosomal dominant trait with reduced penetrance [24▪].
PubMedID- 23142961 Differences in gender and body distribution of tremor between patients with dystonia and tremor and those of patients with essential tremor also suggest that tremor in dystonia and essential tremor are different entities.
PubMedID- 23450143 A relevant example is et-like arm tremor with cervical dystonia, a phenotype of highly contested classification (see schiebler et al137 for review).
PubMedID- 23775978 Those affected in the family exhibited focal cervical dystonia, occasionally with mild tremor, having its onset in early adulthood to late midlife (18–66 years of age).
PubMedID- 23222958 It is defined by the presence of dystonia (with or without tremor) as the only neurologic sign, as well as the absence of historical, imaging or laboratory findings suggesting an acquired cause or non-primary form of dystonia (e.g.
PubMedID- 21692111 Early postoperative management in deep brain stimulation-treated patients with dystonia differs from that of patients with essential tremor and parkinson's disease, mainly due to the usually delayed effects of deep brain stimulation and the heterogenous clinical manifestation and etiologies of dystonia.
PubMedID- 23439931 Frequencies range from 1 to 6 hz during dystonic contractions, with higher frequencies similar to et seen during voluntary movements.4 tremor associated with dystonia (occurring in a clinically non-dystonic body part in a patient with dystonia) can also occur.47 characteristic of dt is the null point, a position in which the tremor almost fully abates.65 it may initially be present during specific action but can generalize to occur with any task.

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