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
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Scientists launch major study to unlock secrets of deadly batten disease
Knowledge-focused Recruiting nowThis study follows 300 people with CLN3 Batten disease, a rare genetic disorder that causes vision loss, seizures, and decline in thinking and movement. Researchers collect samples like blood and spinal fluid to find biological markers that could be used in future treatment trial…
Sponsor: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) • Aim: Knowledge-focused
Last updated Sep 10, 2026 00:00 UTC
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New italian registry aims to unlock secrets of rare brain disease
Knowledge-focused Recruiting nowThis study is building a registry of 50 people with NCL, a rare and severe brain disorder. Researchers will collect detailed clinical data, biomarkers, and patient-reported outcomes over time. The goal is to better understand the disease's natural history and develop tools that c…
Sponsor: IRCCS Fondazione Stella Maris • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:01 UTC
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Scientists track batten disease to unlock its secrets
Knowledge-focused Recruiting nowThis study follows 500 children and adults with Batten disease to learn how the condition naturally changes over time. Researchers will measure movement, thinking, behavior, and daily function using a special rating scale. The goal is to better understand the disease and improve …
Sponsor: University of Rochester • Aim: Knowledge-focused
Last updated Jun 26, 2026 15:36 UTC