Juvenile neuronal ceroid lipofuscinosis

MONDO:0019262

A genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) typically characterized by onset at early school age with vision loss due to retinopathy, seizures and the decline of mental and motor capacities.

Also known as: JNCL, Spielmeyer-Vogt disease, batten disease, juvenile NCL, juvenile neuronal ceroid lipofuscinosis

6 clinical trials for this condition and its sub-types, 6 tagged with Juvenile 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 Juvenile neuronal ceroid lipofuscinosis

Juvenile neuronal ceroid lipofuscinosis 1 0 trials
Juvenile neuronal ceroid lipofuscinosis 10 0 trials
Juvenile neuronal ceroid lipofuscinosis 2 0 trials
Juvenile neuronal ceroid lipofuscinosis 3 0 trials
Juvenile neuronal ceroid lipofuscinosis 5 0 trials
Juvenile neuronal ceroid lipofuscinosis 6 0 trials
Neuronal ceroid lipofuscinosis 9 0 trials
Parkinsonism due to ATP13A2 deficiency 0 trials

Including sub-types (6) Tagged with Juvenile neuronal ceroid lipofuscinosis (6)

Trials to join now! 1 Not yet recruiting 1 Not yet finished but already full! 3 Completed 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

Juvenile neuronal ceroid lipofuscinosis

Where it sits in the disease tree

Scientists launch major study to unlock secrets of deadly batten disease