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Late infantile neuronal ceroid lipofuscinosis

Late infantile neuronal ceroid lipofuscinoses (LINCLs) are a genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs; see this term) typically characterized by onset during infancy or early childhood with decline of mental and motor capacities, epilepsy, and vision loss through retinal degeneration.

Motor deterioration

Loss of previously present motor (i.e., movement) abilities.

Total: 1

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PMID (PMCID)
27343025	FEMALE
	Chorea in Late-Infantile Neuronal Ceroid Lipofuscinosis: AnAtypical Presentation.
	Saini AG, Sankhyan N, Singhi P. Pediatr Neurol. 2016;60:75-8.
	Classic late-infantile neuronal ceroid lipofuscinosis is characterized by progressive intellectual and motor deterioration, seizures, vision loss, and early death.