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Late infantile neuronal ceroid lipofuscinosis 10

MONDO:0979372

Also known as: late infantile CLN10 disease

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (680) Metabolic disease (233) Nervous system disorder (231) Inherited lipid metabolism disorder (189) Hereditary disease (176) Neurodegenerative disease (171) Central nervous system disorder (107) Inborn errors of metabolism (45) Lysosomal storage disease (35) Human disease (14)
Trials to join now! 1
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  • 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 Jun 27, 2026 09:08 UTC

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