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Neuronal Ceroid-LipofuscinosesLegal notice  


Other terms
Neuronal Ceroid Lipofuscinoses,Neuronal Ceroid-Lipofuscinosis,Ceroid-Lipofuscinosis, Neuronal,Ceroid Lipofuscinosis, Neuronal,Lipofuscinosis, Neuronal Ceroid,Neuronal Ceroid Lipofuscinosis,Late-Infantile Neuronal Ceroid Lipofuscinosis,Late Infantile Neuronal Ceroid Lipofuscinosis,Neuronal Ceroid Lipofuscinosis, Late-Infantile,Neuronal Ceroid Lipofuscinosis, Late Infantile,Jansky-Bielschowsky Disease,Jansky Bielschowsky Disease,Juvenile Neuronal Ceroid Lipofuscinosis,Juvenile Cerebroretinal Degeneration,Cerebroretinal Degeneration, Juvenile,Cerebroretinal Degenerations, Juvenile,Juvenile Cerebroretinal Degenerations,Neuronal Ceroid Lipofuscinosis, Juvenile,Batten-Mayou Disease,Batten Mayou Disease,Spielmeyer-Vogt Disease,Spielmeyer Vogt Disease,Batten-Spielmeyer-Vogt Disease,Batten Spielmeyer Vogt Disease,Batten Disease,Adult Neuronal Ceroid Lipofuscinosis,Kufs Disease,Neuronal Ceroid Lipofuscinosis, Adult,Infantile Neuronal Ceroid Lipofuscinosis,Santavuori-Haltia Disease,Santavuori Haltia Disease,Neuronal Ceroid Lipofuscinosis, Infantile

Description
Neuronal Ceroid-Lipofuscinoses: A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure.



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