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  2. Sensory neuronopathy - Wikipedia

    en.wikipedia.org/wiki/Sensory_neuronopathy

    Sensory neuronopathy (also known as sensory ganglionopathy) is a type of peripheral neuropathy that results primarily in sensory symptoms (such as parasthesias, pain or ataxia) due to destruction of nerve cell bodies in the dorsal root ganglion. [1]

  3. Autoimmune autonomic ganglionopathy - Wikipedia

    en.wikipedia.org/wiki/Autoimmune_autonomic...

    Autoimmune autonomic ganglionopathy is a type of immune-mediated autonomic failure that is associated with antibodies against the ganglionic nicotinic acetylcholine receptor present in sympathetic, parasympathetic, and enteric ganglia. Typical symptoms include gastrointestinal dysmotility, orthostatic hypotension, and tonic pupils. [1]

  4. Peripheral neuropathy - Wikipedia

    en.wikipedia.org/wiki/Peripheral_neuropathy

    Peripheral neuropathy may be classified according to the number and distribution of nerves affected (mononeuropathy, mononeuritis multiplex, or polyneuropathy), the type of nerve fiber predominantly affected (motor, sensory, autonomic), or the process affecting the nerves; e.g., inflammation (), compression (compression neuropathy), chemotherapy (chemotherapy-induced peripheral neuropathy).

  5. Megavitamin-B6 syndrome - Wikipedia

    en.wikipedia.org/wiki/Megavitamin-B6_syndrome

    [23] [3] It is classified as a sensory ganglionopathy due to involvement of these ganglia. [61] [b] In electrodiagnostic testing, it has characteristic non-length-dependent abnormalities of sensory action potentials that occur globally, rather than distally decreasing sensory nerve action potential amplitudes. [57]

  6. Facial onset sensory and motor neuronopathy - Wikipedia

    en.wikipedia.org/wiki/Facial_onset_sensory_and...

    Facial onset sensory and motor neuronopathy, often abbreviated FOSMN, is a rare disorder of the nervous system in which sensory and motor nerves of the face and limbs progressively degenerate over a period of months to years. This degenerative process, the cause of which is unknown, eventually results in sensory and motor symptoms — the ...

  7. Hereditary sensory and autonomic neuropathy - Wikipedia

    en.wikipedia.org/wiki/Hereditary_sensory_and...

    Hereditary sensory neuropathy type 1 is a condition characterized by nerve abnormalities in the legs and feet (peripheral neuropathy). Many people with this condition have tingling, weakness, and a reduced ability to feel pain and sense hot and cold.

  8. Trigeminal nerve - Wikipedia

    en.wikipedia.org/wiki/Trigeminal_nerve

    Sensory neuronopathy (also known as sensory ganglionopathy) is a type of peripheral neuropathy in which sensory nerve cell bodies in the dorsal root ganglia, commonly including the trigeminal ganglion of the trigeminal nerve, are damaged due to a variety of mechanisms leading to sensory symptoms such as parasthesias, dysesthesias, or ...

  9. Dorsal root ganglion - Wikipedia

    en.wikipedia.org/wiki/Dorsal_root_ganglion

    The cell bodies of sensory neurons known as first-order neurons are located in the dorsal root ganglia. [2] The axons of dorsal root ganglion neurons are known as afferents. In the peripheral nervous system, afferents refer to the axons that relay sensory information into the central nervous system (i.e. the brain and the spinal cord).