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  2. Dysdiadochokinesia - Wikipedia

    en.wikipedia.org/wiki/Dysdiadochokinesia

    Dysdiadochokinesia is also seen in Friedreich's ataxia and multiple sclerosis, as a cerebellar symptom (including ataxia, intention tremor and dysarthria). It is also a feature of ataxic dysarthria. Dysdiadochokinesia often presents in motor speech disorders , therefore testing for dysdiadochokinesia can be used for a differential diagnosis.

  3. Dysarthria - Wikipedia

    en.wikipedia.org/wiki/Dysarthria

    Ataxic dysarthria is an acquired neurological and sensorimotor speech deficit. It is a common diagnosis among the clinical spectrum of ataxic disorders. [ 9 ] Since regulation of skilled movements is a primary function of the cerebellum , damage to the superior cerebellum and the superior cerebellar peduncle is believed to produce this form of ...

  4. Spinocerebellar ataxia type 1 - Wikipedia

    en.wikipedia.org/wiki/Spinocerebellar_ataxia_type_1

    Many ataxic disorders which were historically identified as Marie's ataxia, olivopontocerebellar atrophy or other names were now reclassified as types of spinocerebellar ataxia, each type numbered in order as a new locus was found. [76] In 1993, the gene and a mutation causing spinocerebellar ataxia type 1 was identified.

  5. Progressive supranuclear palsy - Wikipedia

    en.wikipedia.org/wiki/Progressive_supranuclear_palsy

    Patients with PSP usually seek or are referred to occupational therapy, speech-language pathology for motor speech changes (typically a spastic-ataxic dysarthria), and physical therapy for balance and gait problems with reports of frequent falls. [50] There has been research in the use of robot-assisted gait training. [51]

  6. Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis

    en.wikipedia.org/wiki/Sensory_ataxic_neuropathy...

    This disorder is characterized by the adult-onset triad consisting of the following symptoms: sensory ataxic neuropathy, dysarthria, and ophthalmoparesis. MRIS often reveals white matter abnormalities and bilateral thalamus lesions. Other symptoms include generalized myopathy, epilepsy, and deafness. [1] [2]

  7. Spinocerebellar ataxia type 6 - Wikipedia

    en.wikipedia.org/wiki/Spinocerebellar_ataxia_type_6

    Spinocerebellar ataxia type 6 (SCA6) is a rare, late-onset, autosomal dominant disorder, which, like other types of SCA, is characterized by dysarthria, oculomotor disorders, peripheral neuropathy, and ataxia of the gait, stance, and limbs due to cerebellar dysfunction. Unlike other types, SCA 6 is not fatal.

  8. Scanning speech - Wikipedia

    en.wikipedia.org/wiki/Scanning_speech

    Scanning speech is a type of ataxic dysarthria in which spoken words are broken up into separate syllables, often separated by a noticeable pause, and spoken with varying force. [1] The sentence "Walking is good exercise", for example, might be pronounced as "Walk (pause) ing is good ex (pause) er (pause) cise".

  9. 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 ]