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Infantile neuronal ceroid lipofuscinosis
rareA form of neuronal ceroid lipofuscinosis (NCL) characterized by onset during the second half of the first year of life and rapid mental and motor deterioration leading to loss of all psychomotor abilities.
- Identifiers
- MONDO:0019261 Orphanet:79263
- Also known as
- Classic Infantile CLN1 Disease · Hagberg-Santavuori disease · INCL · infantile NCL · Santavuori disease
Subtypes
Rare disease
Projects
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