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  2. Dysmetria - Wikipedia

    en.wikipedia.org/wiki/Dysmetria

    Researchers now are testing different possibilities for treating dysmetria and ataxia. One opportunity for treatment is called rehearsal by eye movement. [14] It is believed that visually guided movements require both lower- and higher-order visual functioning by first identifying a target location and then moving to acquire what is sought ...

  3. Ataxia - Wikipedia

    en.wikipedia.org/wiki/Ataxia

    Ataxia (from Greek α- [a negative prefix] + -τάξις [order] = "lack of order") is a neurological sign consisting of lack of voluntary coordination of muscle movements that can include gait abnormality, speech changes, and abnormalities in eye movements, that indicates dysfunction of parts of the nervous system that coordinate movement, such as the cerebellum.

  4. Spinocerebellar ataxia type 1 - Wikipedia

    en.wikipedia.org/wiki/Spinocerebellar_ataxia_type_1

    Overall, physical therapy for individuals with ataxia has modest evidence supporting its efficaciousness, but current practice uses custom treatments without a standard decision making procedure between clinics, which limits the ability to reproducibly assess the quality of routines in literature. [56]

  5. Cerebellar ataxia - Wikipedia

    en.wikipedia.org/wiki/Cerebellar_ataxia

    Cerebellar ataxia is a form of ataxia originating in the cerebellum. [1] Non-progressive congenital ataxia (NPCA) is a classical presentation of cerebral ataxias. Cerebellar ataxia can occur as a result of many diseases and may present with symptoms of an inability to coordinate balance, gait, extremity and eye movements. [ 2 ]

  6. Spinocerebellar ataxia - Wikipedia

    en.wikipedia.org/wiki/Spinocerebellar_ataxia

    As with other forms of ataxia, SCA frequently results in atrophy of the cerebellum, [5] loss of fine coordination of muscle movements leading to unsteady and clumsy motion, and other symptoms. Ocular deficits can be quantified using the SODA scale. [6] The symptoms of an ataxia vary with the specific type and with the individual patient.

  7. Autosomal dominant leukodystrophy with autonomic disease

    en.wikipedia.org/wiki/Autosomal_dominant_leuko...

    After these symptoms start, movement impairments develop; they start off at the legs but then progress and move to the arms and the face, these impairments include either muscular spasticity or weakness, intention tremors, ataxia, dysmetria, and dysdiadochokinesis. [9] [8] [11] [10] In some individuals, progressive dementia is present. [8] [9] [11]

  8. Intention tremor - Wikipedia

    en.wikipedia.org/wiki/Intention_tremor

    Patients with intention tremors usually complain of difficulties with activities of daily living, including drinking from a cup, grabbing utensils to eat, and problems with coordination eye to an object or ambulation. Associated cerebellar signs can include nystagmus, dysmetria, dysdiadochokinesia, hypotonia, proprioception deficits, and gait ...

  9. Autosomal recessive cerebellar ataxia type 1 - Wikipedia

    en.wikipedia.org/wiki/Autosomal_recessive...

    In most cases, between the age of 2 and 4 oculomotor signals are present. Between the age of 2 and 8, telangiectasias appears. Usually by the age of 10 the child needs a wheel chair. Individuals with autosomal recessive cerebellum ataxia usually survive until their 20s; in some cases individuals have survived until their 40s or 50s. [citation ...

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