Washington, August 13 (ANI): Scientists have discovered a gene mutation that may be linked to the development of juvenile amyotrophic lateral sclerosis (ALS), also referred to as Lou Gehrig's disease.
Juvenile ALS-characterized by age of onset below 25 years-is a rare and sporadic disorder, leading to paralysis and eventual death from respiratory failure.esearchers in Saudi Arabia found a specific gene mutation in these patients - and believe it could play a significant role in the disease.
The next step is creating drugs that can target the mutation.
The study was recently published in Annals of Neurology, a journal of the American Neurological Association and the Child Neurology Society. (ANI)
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