Late infantile neuronal ceroid lipofuscinosis (Q89128): Difference between revisions

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Latest revision as of 15:40, 15 August 2026

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

Language	Label	Description	Also known as
default for all languages	ID_1923920542
English	Late infantile neuronal ceroid lipofuscinosis	Late infantile neuronal ceroid lipofuscinoses are a genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) typically characterised by onset during infancy or early childhood with decline of mental and motor capacities, epilepsy, and vision loss through retinal degeneration.