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  2. Extrapyramidal symptoms - Wikipedia

    en.wikipedia.org/wiki/Extrapyramidal_symptoms

    Medications are used to reverse the symptoms of extrapyramidal side effects caused by antipsychotics or other drugs, by either directly or indirectly increasing dopaminergic neurotransmission. The treatment varies by the type of the EPS, but may involve anticholinergic agents such as procyclidine, benztropine, diphenhydramine, and trihexyphenidyl.

  3. Dysarthria - Wikipedia

    en.wikipedia.org/wiki/Dysarthria

    Various neurological and motor disorders can give rise to dysarthria. The main causes can be classified as genetic, infectious, toxic, traumatic, vascular, neoplastic, demyelinating, degenerative, or other. [7] [8] Genetic: Wilson's disease, Tay–Sachs disease, and Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis (SANDO syndrome)

  4. 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]

  5. Flaccid dysarthria - Wikipedia

    en.wikipedia.org/wiki/Flaccid_dysarthria

    Flaccid dysarthria is a motor speech disorder resulting from damage to peripheral nervous system (cranial or spinal nerves) or lower motor neuron system. Depending on which nerves are damaged, flaccid dysarthria affects respiration, phonation, resonance, and articulation. It also causes weakness, hypotonia (low-muscle tone), and diminished ...

  6. Demyelinating disease - Wikipedia

    en.wikipedia.org/wiki/Demyelinating_disease

    Chronic exposure to neuroleptic medications may also cause demyelination. [3] Furthermore, deficiencies in vitamin B12 can result in dysmyelination. [4] [5] Demyelinating diseases are traditionally classified into two types: demyelinating myelinoclastic diseases and demyelinating leukodystrophic diseases. In the first group, a healthy and ...

  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.

  8. Spinocerebellar ataxia type 1 - Wikipedia

    en.wikipedia.org/wiki/Spinocerebellar_ataxia_type_1

    The success in linking one of these class of diseases to a locus showed that the classification systems in use were unable to distinguish between diseases with many different causes. Many ataxic disorders which were historically identified as Marie's ataxia, olivopontocerebellar atrophy or other names were now reclassified as types of ...

  9. Pseudobulbar palsy - Wikipedia

    en.wikipedia.org/wiki/Pseudobulbar_palsy

    Since pseudobulbar palsy is a syndrome associated with other diseases, treating the underlying disease may eventually reduce the symptoms of pseudobulbar palsy. [ citation needed ] Possible pharmacological interventions for pseudobulbar affect include the tricyclic antidepressants , serotonin reuptake inhibitors , and a novel approach utilizing ...

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