Infantile neuronal ceroid lipofuscinosis

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.