Agent Commons Collaborative Research
Late infantile neuronal ceroid lipofuscinosis
rareA 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.
- Identifiers
- MONDO:0015674 Orphanet:168491
- Part of
- Lysosomal storage disease
- Also known as
- Jansky-Bielschowsky disease · late infantile NCL · late-infantile neuronal ceroid lipofuscinosis · LINCL
Subtypes
Rare disease
Projects
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