Neuronal ceroid lipofuscinosis
MONDO:0016295A 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.
Also known as: NCL, ceroid lipofuscinoses, neuronal ceroid lipofuscinosis
23 clinical trials for this condition and its sub-types, 6 tagged with Neuronal ceroid lipofuscinosis itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Neuronal ceroid lipofuscinosis
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Neuronal ceroid lipofuscinosis 3 12 trials
2 sub-types
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Neuronal ceroid lipofuscinosis 2 8 trials
3 sub-types
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8 sub-types
- Juvenile neuronal ceroid lipofuscinosis 1 0 trials
- Juvenile neuronal ceroid lipofuscinosis 10 0 trials
- Juvenile neuronal ceroid lipofuscinosis 2 0 trials
- Juvenile neuronal ceroid lipofuscinosis 3 0 trials
- Juvenile neuronal ceroid lipofuscinosis 5 0 trials
- Juvenile neuronal ceroid lipofuscinosis 6 0 trials
- Neuronal ceroid lipofuscinosis 9 0 trials
- Parkinsonism due to ATP13A2 deficiency 0 trials
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Ceroid lipofuscinosis, neuronal, 6A 4 trials
2 sub-types
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Neuronal ceroid lipofuscinosis 7 2 trials
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Neuronal ceroid lipofuscinosis 8 1 trial · 2 incl. sub-types
2 sub-types
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Neuronal ceroid lipofuscinosis 1 1 trial
4 sub-types
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3 sub-types
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Neuronal ceroid lipofuscinosis 5 1 trial
3 sub-types
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Adult neuronal ceroid lipofuscinosis 0 trials
5 sub-types
- Adult neuronal ceroid lipofuscinosis 1 0 trials
- Adult neuronal ceroid lipofuscinosis 5 0 trials
- Ceroid lipofuscinosis, neuronal, 4 (Kufs type) 0 trials
- Neuronal ceroid lipofuscinosis 11 0 trials
- Neuronal ceroid lipofuscinosis 13 0 trials
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2 sub-types