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On page 1 showing 1 ~ 4 term(s) out of 4 term(s)

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    Miller Fisher Syndrome

    Description: A variant of the GUILLAIN-BARRE SYNDROME characterized by the acute onset of oculomotor dysfunction, ataxia, and loss of deep tendon reflexes with relative sparing of strength in the extremities and trunk. The ataxia is produced by peripheral sensory nerve dysfunction and not by cerebellar injury. Facial weakness and sensory loss may also occur. The process is mediated by autoantibodies directed against a component of myelin found in peripheral nerves. (Adams et al., Principles of Neurology, 6th ed, p1313; Neurology 1987 Sep;37(9):1493-8)

    Preferred ID: MESH:M0029456     Type: term      ID# ILX:0737691     Score: 24016.172


    Miller Fisher Syndrome

    Description: A variant of the GUILLAIN-BARRE SYNDROME characterized by the acute onset of oculomotor dysfunction, ataxia, and loss of deep tendon reflexes with relative sparing of strength in the extremities and trunk. The ataxia is produced by peripheral sensory nerve dysfunction and not by cerebellar injury. Facial weakness and sensory loss may also occur. The process is mediated by autoantibodies directed against a component of myelin found in peripheral nerves (MeSH).

    Preferred ID: ILX:0106980     Type: term      ID# ILX:0106980     Score: 23714.875


    Miller Fisher syndrome

    Description: An autoimmune process characterized by the clinical triad of ophthalmoplegia, ataxia, and areflexia.

    Preferred ID: MONDO:0005851     Type: term      ID# ILX:0767863     Score: 22651.623


    Guillain-Barre syndrome

    Description: Guillain-BarrC) syndrome (GBS) is the term used to describe a spectrum of rare post-infectious neuropathies that usually occur in otherwise healthy patients. GBS is clinically heterogeneous and encompasses acute inflammatory demyelinating polyradiculoneuropathy (AIDP), acute motor axonal neuropathy (AMAN) and acute motor-sensory axonal neuropathy (AMSAN), Miller-Fisher syndrome (MFS; see these terms) and some other regional variants.

    Preferred ID: MONDO:0016218     Type: term      ID# ILX:0769552     Score: 131.37718


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