Syndrome Fahr is described as calcification of the basal ganglia and is a rare inherited or sporadic neurological disease with a prevalence of 1:1000000 (1). For the first time described in 1930 in the works of Dr. Karl Theodor Fahr. it is characterized by calcium deposition in areas of the brain to control movement: basal gamma. https://www.markbroyard.com/flash-offer-36-meter-4-teilige-interlock-ettore-rea-c-h-teleskopstange-for-sale-limited-save/