Adult neuronal ceroid lipofuscinosis

A genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) with onset during the third decade of life, characterized by dementia, seizures and loss of motor capacities, and sometimes associated with visual loss caused by retinal degeneration.

Also known as: ANCL, Kufs disease, adult NCL, adult neuronal ceroid lipofuscinosis, neuronal ceroid lipofuscinosis of adults, CLN4 disease, adult autosomal dominant, Kuf's disease, neuronal ceroid lipofuscinosis 4

1 clinical trial for this condition and its sub-types.