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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↑ 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)

Trials to join now! 1

Scientists launch major study to unlock secrets of deadly batten disease

Knowledge-focused Recruiting now

This study follows 300 people with CLN3 Batten disease, a rare genetic disorder that causes vision loss, seizures, and decline in thinking and movement. Researchers collect samples like blood and spinal fluid to find biological markers that could be used in future treatment trial…

Sponsor: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) • Aim: Knowledge-focused

Last updated Sep 10, 2026 00:00 UTC

Infantile neuronal ceroid lipofuscinosis

Where it sits in the disease tree

Scientists launch major study to unlock secrets of deadly batten disease