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Neuronal ceroid lipofuscinosis

A group of inherited progressive degenerative brain diseases characterized clinically by a decline of mental and other capacities, epilepsy, and vision loss through retinal degeneration, and histopathologically by intracellular accumulation of an autofluorescent material, ceroid lipofuscin, in the neuronal cells in the brain and in the retina.

6 trials tagged with this condition →

Neuronal ceroid lipofuscinosis 3 12 trials Sub-types →
Neuronal ceroid lipofuscinosis 2 8 trials Sub-types →
Juvenile neuronal ceroid lipofuscinosis 6 trials Sub-types →
Ceroid lipofuscinosis, neuronal, 6A 4 trials Sub-types →
Neuronal ceroid lipofuscinosis 7 2 trials
Neuronal ceroid lipofuscinosis 8 1 trial · 2 incl. sub-types Sub-types →
Neuronal ceroid lipofuscinosis 1 1 trial Sub-types →
Neuronal ceroid lipofuscinosis 10 1 trial Sub-types →
Neuronal ceroid lipofuscinosis 5 1 trial Sub-types →
Adult neuronal ceroid lipofuscinosis 0 trials Sub-types →
Ceroid lipofuscinosis, neuronal, 6B (Kufs type) 0 trials
Congenital neuronal ceroid lipofuscinosis 0 trials
Infantile neuronal ceroid lipofuscinosis 0 trials Sub-types →
Progressive myoclonic epilepsy type 3 0 trials