Machado-Joseph disease was first described in 1972 among the descendants of Portuguese-Azorean immigrants to the United States, including the family of William Machado
It is named for an American neurologist, Samuel A. K. Wilson, who first described it in 1912.
He is the first person that described the Huntington disease.
George Huntington who was a young physician, first described the disease in 1872.
The disease was first described in the 5th century BC by Hippocrates.
Caused by the GSS prion, this disease was first described in 1928.
It was first described in 1977 and the microbe was identified in 1982.
The disease was first described in the 5th century BC by Hippocrates.
The Norwegian neurologist , Sigvald Refsum first described the disorder in 1946.
The condition was first described by Frederick Lewy in 1941 when he described Lewy bodies, which are abnormal inclusions in the cytoplasm (components of a cell outside the nucleus) of cells found in patients who had Parkinson's disease
Gaucher disease is the most common lysosomal storage disease. It was named for the French physician Phillipe Gaucher who first described it in 1882. The disease is caused by a lack of glucocerebrosidase, which causes a buildup of glucocerebroside in the tissues.
CMT is named for the three neurologists who first described the condition in the late 1800s
Outbreaks of the disease were first described in the 16th century but it has been around for much longer than that.