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196 Possible Causes for Dystonia, focal dystonia becomes segmental or generalized, Truncal Ataxia

Did you mean: Dystonia, focal dystonia, becomes segmental or generalized, Truncal Ataxia

  • Primary Torsion Dystonia

    With a stronger family history, a significantly lower AaO was seen in all focal dystonias.[] Primary torsion dystonia (PTD) is a genetically heterogeneous, isolated form of dystonia.[] Forty-six of them had segmental dystonia and 59 had focal dystonia.[]

  • Adult-Onset Cervical Dystonia Type DYT23

    One family member, II-1,had additional neurological signs on examination: he exhibitedmild truncal ataxia, dysarthria, and mild cognitive impairment,all dating fromanepisodeofWernicke-Korsakoffs[] Related phenotypes are torticollis and cerebellar atrophy Disease Ontology : 12 A focal dystonia characterized by autosomal dominant inheritance of adult-onset cervical dystonia[] […] dystonia Spinocerebellar ataxia with axonal neuropathy type 2 Meckel syndrome Asperger syndrome Antidepressant or antipsychotics toxicity or dose selection Azathioprine or[]

  • Spinocerebellar Ataxia Type 1

    Neurological examination 5 years after onset revealed slow eye movement with nystagmus as well as limb and truncal ataxia.[] Some reports have identified cognitive dysfunction (memory impairment, defects in executive functioning) and focal dystonias (writer's cramp) in the clinical presentation.[] […] entity in patients combining dystonia and cerebellar ataxia.[]

  • Autosomal Recessive Spinocerebellar Ataxia Type 17

    […] the extremities, truncal ataxia, increased reflexes in the lower extremities, and intellectual disability.[] Focal dystonia as a presenting sign of spinocerebellar ataxia 17.[] The book is divided into sections on Parkinson's disease, Huntington's disease, dystonia, tremor, paroxysmal movement disorders, ataxia, myoclonus, restless legs syndrome,[]

  • Ataxia

    […] and presence of subtle truncal ataxia.[] Similar to pure ataxia, pure focal dystonia (torticollis) can be the only presenting symptom of SCA3.[] We report on a 61-year-old woman and on a 55-year-old man who had history of recent fever, who were hospitalized because of acute severe truncal ataxia, opsoclonus and tremor[]

  • Spastic Ataxia with Congenital Miosis

    Midline lesions can produce severe gait and truncal ataxia.[] Skeletal muscle atrophy Tremor Aplasia/Hypoplasia of the cerebellum Peripheral neuropathy Glaucoma Muscular hypotonia Lower limb hypertonia Clumsiness Difficulty running Focal[] , DYT13 type Primary dystonia, DYT17 type Primary dystonia, DYT2 type Primary dystonia, DYT21 type Primary dystonia, DYT4 type Primary dystonia, DYT6 type Primary microcephaly-epilepsy-permanent[]

  • Ataxia-Oculomotor Apraxia Syndrome

    Subsequently, he suffered from arms dysmetria, truncal ataxia and cerebellar dysarthric speech. He was wheelchair bound by the age of 23-years.[] Autosomal dominant cerebellar ataxia type IV Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome Autosomal dominant dopa-responsive dystonia Autosomal dominant focal[] The predominant sign at onset was gait ataxia in eight patients (57%) and chorea or dystonia in seven (50%).[]

  • Cerebellar Ataxia with Peripheral Neuropathy Type 2

    The vermis is concerned with midline and truncal position and receives input from the spinal cord. Dysfunction is noted by postural instability and gait ataxia.[] Focal dystonia as a presenting sign of spinocerebellar ataxia 17. Mov Disord. 2004 ; 19 (2): 217 –20. 111. Toyoshima Y, Yamada M, Onodera O, et al.[] Polyneuropathy was found in 97.5% of AOA2 patients, cerebellar atrophy in 96%, occasional oculomotor apraxia in 51%, pyramidal signs in 20.5%, head tremor in 14%, dystonia[]

  • X-linked Parkinsonism-Spasticity Syndrome

    Moderate truncal ataxia was present with bilateral dysmetria and dysdiadochokinesia. It was not possible to assess cerebellar function in the legs due to weakness.[] Primary; Mixed Type Autosomal Dominant Adolescent onset, mostly segmental, rarely generalizes DYT-7 18pter-p11.32 Adult Onset Focal Primary Autosomal Dominant Adult onset of focal[] ataxia.[]

  • Neuroferritinopathy

    […] hypotonia, cerebellar ataxia, optic nerve atrophy.[] dystonia.[] Both display a range of different movement disorders including dystonia, chorea, and a Parkinsonian syndrome.[]

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