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  2. ALS - Wikipedia

    en.wikipedia.org/wiki/ALS

    While the disease does not cause pain directly, pain is a symptom experienced by most people with ALS caused by reduced mobility. [36] Symptoms of lower motor neuron degeneration include muscle weakness and atrophy, muscle cramps, and fleeting twitches of muscles that can be seen under the skin (fasciculations). [24]

  3. My Years of Leg Pain Turned Out to Be ALS: Why the ... - AOL

    www.aol.com/lifestyle/years-leg-pain-turned-als...

    ALS is pretty much entirely untreatable, save for a few measures to slow down progression if you're among the 10% with the genetic kind. In those cases, doctors can sometimes target a gene.

  4. Multifocal motor neuropathy - Wikipedia

    en.wikipedia.org/wiki/Multifocal_motor_neuropathy

    Definitive diagnosis is often difficult, and many MMN patients labor for months or years under an ALS diagnosis before finally getting a determination of MMN. MMN usually involves very little pain; however, muscle cramps, spasms and twitches can cause pain for some people. MMN is not fatal, and does not diminish life expectancy.

  5. Denervation - Wikipedia

    en.wikipedia.org/wiki/Denervation

    Following an acute poliovirus infection, symptoms such as fatigue, asthenia, and pain are believed to be linked to muscle denervation. [9] Much like post-polio syndrome, ALS also has similar symptoms of motor neurodegeneration leading to general weakness and, in some cases, paralysis. The type of symptoms experienced can depend on which areas ...

  6. If You Notice This One Thing While You're Eating, Talk to ...

    www.aol.com/lifestyle/notice-one-thing-while...

    Neurological conditions, including Parkinson's disease, stroke, multiple sclerosis or amyotrophic lateral sclerosis (ALS), can interfere with the nerves and muscles that control swallowing.

  7. Motor neuron diseases - Wikipedia

    en.wikipedia.org/wiki/Motor_neuron_diseases

    Some disorders, like ALS, can occur sporadically (85%) or can have a genetic cause (15%) with the same clinical symptoms and progression of disease. [6] UMNs are motor neurons that project from the cortex down to the brainstem or spinal cord. [18] LMNs originate in the anterior horns of the spinal cord and synapse on peripheral muscles. [18]

  8. Primary lateral sclerosis - Wikipedia

    en.wikipedia.org/wiki/Primary_lateral_sclerosis

    Primary lateral sclerosis (PLS) usually presents with gradual-onset, progressive, lower-extremity stiffness and pain due to muscle spasticity. Onset is often asymmetrical. [ 2 ] Although the muscles do not appear to atrophy as in ALS (at least initially), the disabling aspect of PLS is muscle spasticity and cramping, and intense pain when those ...

  9. Polyneuropathy - Wikipedia

    en.wikipedia.org/wiki/Polyneuropathy

    The most common cause is acute inflammatory demyelinating polyneuropathy AIDP, the most common form of Guillain–Barré syndrome [13] (although other causes include chronic inflammatory demyelinating polyneuropathy) [14] Neuronopathy is the result of issues in the peripheral nervous system (PNS) neurons.

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