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Limb-onset ALS begins with weakness in the hands, arms, feet, and/or legs [10] and accounts for about two-thirds of all classical ALS cases. [9] Bulbar-onset ALS begins with weakness in the muscles of speech, chewing, and swallowing [23] and accounts for about 25% of classical ALS cases. [6]
ALS — also known as Lou Gehrig's disease — is a rare degenerative disease that causes progressive paralysis of the muscles. Patients first experience twitching or weakness in a limb, followed ...
Weakness can be symmetric or asymmetric, and it can occur in body parts that are distal, proximal, or both. According to Statland et al., there are three main weakness patterns that are seen in motor neuron diseases, which are: [6] [9] Asymmetric distal weakness without sensory loss (e.g. ALS, PLS, PMA, MMA)
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Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that typically affects adults around 54–67 [1] years of age, although anyone can be diagnosed with the disease. People diagnosed with ALS live on average 2–4 years after diagnosis due to the quick progression of the disease.
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