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Joseph Samaha, Jim Dagher, Shayan Abdollah Zadegan

Huntington’s disease (HD) is a neurodegenerative disease inherited in an autosomal dominant manner. It is caused by an expansion of cytosine, adenine, guanine (CAG) repeats within the huntingtin (HTT) gene, which is located on chromosome 4. This pathological expansion of CAG repeats results in the production of a mutant huntingtin protein with an abnormally long polyglutamine […]

How can neuroimaging help diagnose ALS?

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Published Online: Jun 12th 2014

Individuals with mutations in the superoxide dismutase 1 (SOD1) gene develop brain white matter abnormalities before the onset of symptoms of amyotrophic lateral sclerosis (ALS), according to a new imaging study that was presented here at the AAN Annual Meeting in April. Surprisingly, the changes are in a non-motor area of the brain, leaving researchers to wonder whether they signify a previously unsuspected site of disease onset, or a change with no necessary pathogenic relation to the future neurodegenerative process expected in these individuals.

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