The EuroBiotech Journal (Dec 2017)

Genetics of amyotrophic lateral sclerosis: more than twenty years of studies

  • Mazzini Letizia,
  • Marchi Fabiola De,
  • Corrado Lucia,
  • D’Alfonso Sandra

DOI
https://doi.org/10.24190/ISSN2564-615X/2017/S2.05
Journal volume & issue
Vol. 1, no. s2
pp. 131 – 132

Abstract

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Amyotrophic lateral sclerosis, also known as motor neuron disease or Lou Gehrig’s disease, is an adult-onset neurodegenerative disease that targets motor neurons in the spinal cord, cortex and brain stem. Selective degeneration of corticospinal (upper) and spinal (lower) motor neurons manifests as a linear decline in muscular function, eventually resulting in paralysis, speech and swallowing deficits and death, usually from impaired respiratory function, over a time course of approximately 3-5 years.

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