[HTML][HTML] Central nervous system therapy for lysosomal storage disorders

GM Enns, SL Huhn - Neurosurgical Focus, 2008 - thejns.org
GM Enns, SL Huhn
Neurosurgical Focus, 2008thejns.org
✓ Most lysosomal storage disorders are characterized by progressive central nervous
system impairment, with or without systemic involvement. Affected individuals have an array
of symptoms related to brain dysfunction, the most devastating of which is
neurodegeneration following a period of normal development. The blood–brain barrier has
represented a significant impediment to developing therapeutic approaches to treat brain
disease, but novel approaches—including enzyme replacement, small-molecule, gene, and …
✓ Most lysosomal storage disorders are characterized by progressive central nervous system impairment, with or without systemic involvement. Affected individuals have an array of symptoms related to brain dysfunction, the most devastating of which is neurodegeneration following a period of normal development. The blood–brain barrier has represented a significant impediment to developing therapeutic approaches to treat brain disease, but novel approaches—including enzyme replacement, small-molecule, gene, and cell-based therapies—have given children afflicted by these conditions and those who care for them hope for the future.
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