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Up to: Disorder of carbohydrate transmembrane transport and absorption · Paroxysmal dystonia
Dystonia 9
A dystonia characterized by autosomal dominant inheritance of paroxysmal choreoathetosis and progressive spastic paraplegia, episodes are often precipitated by alcohol, fatigue, or emotional stress that has material basis in heterozygous mutation in the SLC2A1 gene on chromosome 1p34.
This condition has no sub-types.