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  2. Post-viral cerebellar ataxia - Wikipedia

    en.wikipedia.org/wiki/Post-viral_cerebellar_ataxia

    Drug treatment to improve muscle coordination has a low success rate. However, the following drugs may be prescribed: clonazepam, amantadine, gabapentin, or buspirone. Occupational or physical therapy may also alleviate lack of coordination. Changes to diet and nutritional supplements may also help. Treatment will depend on the cause.

  3. Acute disseminated encephalomyelitis - Wikipedia

    en.wikipedia.org/wiki/Acute_disseminated...

    Acute disseminated encephalomyelitis (ADEM), or acute demyelinating encephalomyelitis, is a rare autoimmune disease marked by a sudden, widespread attack of inflammation in the brain and spinal cord. As well as causing the brain and spinal cord to become inflamed, ADEM also attacks the nerves of the central nervous system and damages their ...

  4. Immunoglobulin therapy - Wikipedia

    en.wikipedia.org/wiki/Immunoglobulin_therapy

    Immunoglobulin therapy is the use of a mixture of antibodies (normal human immunoglobulin) to treat several health conditions. [13] [14] These conditions include primary immunodeficiency, immune thrombocytopenic purpura, chronic inflammatory demyelinating polyneuropathy, Kawasaki disease, certain cases of HIV/AIDS and measles, Guillain–Barré syndrome, and certain other infections when a ...

  5. Progressive inflammatory neuropathy - Wikipedia

    en.wikipedia.org/wiki/Progressive_inflammatory...

    Removal from exposure was the first line of treatment. Due to the progressive sensory loss and weakness, various medications were often required. These included intravenous methylprednisolone, oral prednisone, azathioprine, and/or IVIG. [7] All 24 patients improved, including 7 who received no treatment and 17 who required immunosuppressive ...

  6. Inflammatory demyelinating diseases of the central nervous ...

    en.wikipedia.org/wiki/Inflammatory_demyelinating...

    Inflammatory demyelinating diseases (IDDs), sometimes called Idiopathic (IIDDs) due to the unknown etiology of some of them, are a heterogenous group of demyelinating diseases - conditions that cause damage to myelin, the protective sheath of nerve fibers - that occur against the background of an acute or chronic inflammatory process.

  7. Neuroinflammation - Wikipedia

    en.wikipedia.org/wiki/Neuroinflammation

    Neuroinflammation is widely regarded as chronic, as opposed to acute, inflammation of the central nervous system. [5] Acute inflammation usually follows injury to the central nervous system immediately, and is characterized by inflammatory molecules, endothelial cell activation, platelet deposition, and tissue edema. [6]

  8. Susac's syndrome - Wikipedia

    en.wikipedia.org/wiki/Susac's_syndrome

    A concern about this illness is that it mimics multiple sclerosis when looking at the vision loss and brain lesions. If close attention is not paid to the retina of a patient with vision loss and brain lesions, their symptoms may be mistaken for MS instead of Susac's syndrome. This may account for the low prevalence of the illness.

  9. Neuromyelitis optica spectrum disorder - Wikipedia

    en.wikipedia.org/wiki/Neuromyelitis_optica...

    The most common initial manifestation of the disease is inflammation of the spinal cord (myelitis). [4] Myelitis causes spinal cord dysfunction, which can result in muscle weakness, paralysis in the limbs, lost or reduced sensation, spasms, loss of bladder and bowel control, or erectile dysfunction.