Autosomal dominant striatal neurodegeneration type 1

Autosomal dominant striatal degeneration is a neurologic disorder characterized by variable movement abnormalities due to dysfunction in the striatal part of the basal ganglia.

Also known as: ADSD1, PDE8B striatal degeneration, autosomal dominant, striatal Degeneration, autosomal dominant 1, striatal degeneration, autosomal dominant 1, striatal degeneration, autosomal dominant caused by mutation in PDE8B, ADSD, autosomal dominant striatal neurodegeneration, striatal degeneration, autosomal dominant

24 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant striatal neurodegeneration type 1 itself.