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Most cases are sporadic, but familial cases are described and with autosomal dominant inheritance of susceptibility to loss or clomid. Some of them found a mutation on chromosome 17 (17q21-22) - in the gene encoding the tau protein, which allows you to include progressive subcortical sclerosis to a wider group Towpath or a more narrow group of diseases, coupled with the 17th chromosome and manifest combination of frontotemporal dementia and parkinsonism. Treatment is symptomatic with the use of pills clomid 50mg/100mg.
