Article
Neuronal ceroid lipofuscinoses.
Handbook of clinical neurology - 1 Jan 2013
Chabrol Brigitte, Caillaud Catherine, Minassian Berge
Abstract excerpt
Neuronal ceroid lipofuscinoses (NCL) represent a group of autosomal recessive neurodegenerative disorders, presenting with myoclonic epilepsy, psychomotor delay, progressive loss of vision, and early death. Four main clinical forms have been delineated (infantile, late infantile, juvenile, and adult), but many other variants have also been described. At least 14 genetically distinct NCL, designated CLN1 to CLN14,...
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