Machado Joseph disease

var gaJsHost = (("https:" == document.location.protocol) ? "https://ssl." : "http://www."); document.write(unescape("%3Cscript src='" + gaJsHost + "google-analytics.com/ga.js' type='text/javascript'%3E%3C/script%3E")); aka MJD, spinocerebellar ataxia type 3features adult onset, autosomal dominantUMN and LMN signs resembling ALS may include tongue fasciculations, dystonia, rigidity, progressive external opthalmoplegia, and peripheral neuropathy.Due to CAG triplicate repeat on chromosome 14q32.1Cramping is far more common than in PN or SMA but not ALS and is relieved almost completely by mexilitene, supporting notion that is due to sodium conductance.var pageTracker = _gat._getTracker("UA-3639768-12"); pageTracker._initData(); pageTracker._trackPageview();
Source: neurologyminutiae - Category: Neurologists Source Type: blogs