ceroid-lipofuscinosis

ceroid-lipofuscinosis
neuronal ceroid-lipofuscinosis a term for several genetic lipidoses of diverse biochemical and clinical characteristics, all characterized by progressive neurodegeneration, loss of vision, and a fatal course; the infantile type is Haltia-Santavuori disease; the late infantile type is Jansky-Bielschowsky disease; the juvenile type is Vogt-Spielmeyer disease; and the adult type is Kufs disease.

Medical dictionary. 2011.

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  • CLN5 — Ceroid lipofuscinosis, neuronal 5, also known as CLN5, is a human gene.cite web | title = Entrez Gene: CLN5 ceroid lipofuscinosis, neuronal 5| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=1203| accessdate …   Wikipedia

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