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66 Possible Causes for Mild Sensory Axonal Neuropathy

  • Vasculitis

    Rituxan Neuropathy with IgG or polyclonal IgM binding to Sulfatide Clinical Features Sensory Symmetric; Paraesthesias Distal; Hands & feet Motor loss: Mild or absent Electrophysiology[neuromuscular.wustl.edu] Axonal loss Serum Autoantibody: IgM or IgG vs Sulfatide Serum M-Protein : Occasional Treatment: Cyclophosphamide & Plasma exchange Polyneuropathy & IgM anti-sulfatide antibodies[neuromuscular.wustl.edu]

  • Paraneoplastic Syndrome

    : Panmodal sensory loss; Paresthesias Weakness: Distal & Proximal with sparing of intermediate muscles Mild distal weakness 2 axonal neuropathy: Less prominent than sensory[neuromuscular.wustl.edu] : More common later in disease course than at onset 100% with weight loss 15% Electrophysiological change: 30% to 40% Clinical Distribution: Distal; Legs Arms; Symmetric Sensory[neuromuscular.wustl.edu]

  • Bickerstaff Brainstem Encephalitis

    Supportive evidences include relatively mild sensory loss, cranial neuropathy, and neurophysiological changes involving demyelination or axonal damage in peripheral nerves[bmcresnotes.biomedcentral.com] sensory loss; cranial neuropathy; EMG showing demyelination or axonal damage in peripheral nerves and spinal roots Odaka and his colleagues [ 8 ] reviewed clinical profiles[bmcresnotes.biomedcentral.com] Albuminocytological dissociation in the CSF; anti-GQ1b IgG antibody in serum GBS Acute symmetrical limb weakness and areflexia Albuminocytological dissociation in the CSF; relatively mild[bmcresnotes.biomedcentral.com]

  • Distal Hereditary Motor Neuropathy Type 1

    Charcot-Marie-Tooth hereditary neuropathy type 2 (CMT2) is a non-demyelinating (axonal) peripheral neuropathy characterized by distal muscle weakness and atrophy, mild sensory[bcbst.com] Hereditary Sensory & Autonomic Neuropathies (HSAN) Hereditary Sensory & Autonomic Neuropathies (HSAN) type IV Clinically: Congenital insensitivity to pain Anhidrosis Recurrent[slideshare.net] […] fever Self mutilating behaviour Mild MR Loss of C axons Electrophysiology: SNAP are preserved Biopsy: Sural N biopsy : loss of myelinted & unmyelinated axons 32.[slideshare.net]

  • CANOMAD Syndrome

    Rituxan Neuropathy with IgG or polyclonal IgM binding to Sulfatide Clinical Features Sensory Symmetric; Paraesthesias Distal; Hands & feet Motor loss: Mild or absent Electrophysiology[neuromuscular.wustl.edu] Axonal loss Serum Autoantibody: IgM or IgG vs Sulfatide Serum M-Protein : Occasional Treatment: Cyclophosphamide & Plasma exchange Polyneuropathy & IgM anti-sulfatide antibodies[neuromuscular.wustl.edu]

  • Miller-Fisher Syndrome

    Nerve conduction studies were indicative of a predominantly axonal sensori-motor peripheral neuropathy.[ncbi.nlm.nih.gov] Neurological examination revealed a bilateral external ophthalmoplegia, dysphagia, dysarthria, mild shoulder girdle muscle weakness and gait ataxia, accompanied by absent[ncbi.nlm.nih.gov]

  • Arachnoiditis

    Neuropathy Onset: Acute Clinical Symmetric Distal Legs Arms Course: Mild or no improvement Electrophysiology: Axon loss Nerve pathology: Axon loss Associated syndrome: Rhabdomyolysis[neuromuscular.wustl.edu] Onset: Pain; Allodynia Weakness: Distribution Lumbosacral or Brachial Proximal Single extremity Asymmetric Course Persistent proximal weakness Pain resolution over months Sensory-Motor[neuromuscular.wustl.edu]

  • Acute Pandysautonomia

    Most cases are caused by acute inflammatory demyelinating polyradiculoneuropathy (AIDP), but some are caused by acute motor axonal neuropathy (AMAN) or acute motor and sensory[cidpusa.org] […] or more limbs reaching a maximum within four weeks, reduced or absent tendon reflexes in the weak limbs, and exclusion of alternative causes (box 1).2 Somecases may be so mild[cidpusa.org]

  • Guillain-Barré Syndrome

    In acute motor–sensory axonal neuropathy, there is clear involvement of the sensory fibers, but detailed studies have suggested that mild changes occur in the sensory nerves[geneticaysexologiaintegral.blogspot.com] […] of some patients with acute motor axonal neuropathy.34 Acute motor-conduction-block neuropathy is a mild form of acute motor axonal neuropathy but does not progress to axonal[geneticaysexologiaintegral.blogspot.com]

  • Cerebellar Neoplasm

    : Panmodal sensory loss; Paresthesias Weakness: Distal & Proximal with sparing of intermediate muscles Mild distal weakness 2 axonal neuropathy: Less prominent than sensory[neuromuscular.wustl.edu] : More common later in disease course than at onset 100% with weight loss 15% Electrophysiological change: 30% to 40% Clinical Distribution: Distal; Legs Arms; Symmetric Sensory[neuromuscular.wustl.edu]

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