Late infantile neuronal ceroid lipofuscinosis
MONDO:0015674A genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) typically characterized by onset during infancy or early childhood with decline of mental and motor capacities, epilepsy, and vision loss through retinal degeneration.
Also known as: Jansky-Bielschowsky disease, LINCL, late infantile NCL, late-infantile neuronal ceroid lipofuscinosis, Bielschowsky-jansky disease, Bielschowsky-jansky type neuronal ceroid lipofuscinosis, amaurotic idiocy early juvenile type, amaurotic idiocy late infantile type
5 clinical trials for this condition and its sub-types, 1 tagged with Late infantile 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 Late infantile neuronal ceroid lipofuscinosis
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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 5 1 trial
3 sub-types