Juvenile neuronal ceroid lipofuscinosis
MONDO:0019262A genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) typically characterized by onset at early school age with vision loss due to retinopathy, seizures and the decline of mental and motor capacities.
Also known as: JNCL, Spielmeyer-Vogt disease, batten disease, juvenile NCL, juvenile neuronal ceroid lipofuscinosis
6 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Juvenile neuronal ceroid lipofuscinosis 1
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Juvenile neuronal ceroid lipofuscinosis 10
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Juvenile neuronal ceroid lipofuscinosis 2
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Juvenile neuronal ceroid lipofuscinosis 3
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Juvenile neuronal ceroid lipofuscinosis 5
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Juvenile neuronal ceroid lipofuscinosis 6
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Neuronal ceroid lipofuscinosis 9
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Parkinsonism due to ATP13A2 deficiency
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