Infantile neuronal ceroid lipofuscinosis

MONDO:0019261

A 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.

Also known as: Classic Infantile CLN1 Disease, Hagberg-Santavuori disease, INCL, Santavuori disease, Santavuori-Haltia disease, infantile NCL

1 clinical trial for this condition and its sub-types, 0 tagged with Infantile neuronal ceroid lipofuscinosis itself.

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Where it sits in the disease tree

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Part of

↑ Cerebral lipidosis with dementia (38) ↑ Neuronal ceroid lipofuscinosis (23)

Sub-types of Infantile neuronal ceroid lipofuscinosis

Infantile neuronal ceroid lipofuscinosis 1 0 trials
Infantile neuronal ceroid lipofuscinosis 2 0 trials

Including sub-types (1) Tagged with Infantile neuronal ceroid lipofuscinosis (0)

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