By Michael J. Strong
Over the last ten years, there was an expanding reputation that syndromes of frontotemporal disorder (FTD) are a standard prevalence in sufferers with amyotrophic lateral sclerosis (ALS). Such syndromes should be found in as many as 60% of sufferers with ALS. Conversely, the prevalence of motor neuron disorder in sufferers with clinically natural frontotemporal dementia is more and more famous. this means that to a point there are overlapping syndromes during which either ALS and FTD happen in the similar person.
This quantity summarizes the advances in our figuring out of those issues, in addition to the aptitude courting among the 2. Key themes comprise advances in our skill to clinically describe the frontotemporal syndromes, preclinical detection, neuroimaging, and genetics. The exploding box of recent markers in neuropathology is tested, as is the function of latest genetic mutations in DNA/RNA shipping structures. This publication is the fundamental reference textual content for this subject, and may be of curiosity to neurologists and neurological trainees with a scientific or study curiosity within the FTDs or ALS, neuropsychologists, neuropathologists, and researchers.
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Extra info for Amyotrophic Lateral Sclerosis and the Frontotemporal Dementias
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