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Feasibility of gene therapy for late neuronal ceroid lipofuscinosis Sondhi D; Hackett NR; Apblett RL; Kaminsky SM; Pergolizzi RG; Crystal RGArch Neurol 2001[Nov]; 58 (11): 1793-8Late infantile neuronal ceroid lipofuscinosis is a progressive childhood neurodegenerative disorder characterized by intracellular accumulation of autofluorescent material resembling lipofuscin in neuronal cells. This report summarizes the new therapies under consideration for late infantile neuronal ceroid lipofuscinosis, with a focus on strategies for in vivo gene therapy for the retinal and central nervous system manifestations of the disease.|*Genetic Therapy[MESH]|Adult[MESH]|Aminopeptidases[MESH]|Animals[MESH]|Child[MESH]|Child, Preschool[MESH]|Clinical Trials as Topic[MESH]|Dipeptidyl-Peptidases and Tripeptidyl-Peptidases[MESH]|Endopeptidases/*genetics/therapeutic use[MESH]|Genetic Vectors[MESH]|Humans[MESH]|Neuronal Ceroid-Lipofuscinoses/*genetics/*therapy[MESH]|Serine Proteases[MESH]|Stem Cell Transplantation[MESH]|Tripeptidyl-Peptidase 1[MESH] |
