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    Neurology. 2005 Feb 22;64(4):740-2.

    A CLN5 mutation causing an atypical neuronal ceroid lipofuscinosis of juvenile onset.

    Pineda-Trujillo N, Cornejo W, Carrizosa J, Wheeler RB, Múnera S, Valencia A, Agudelo-Arango J, Cogollo A, Anderson G, Bedoya G, Mole SE, Ruíz-Linares A.

    Genetica Molecular, Facultad de Medicina, Universidad de Antioquia, Medellin, Colombia.

    Three related patients from Colombia presented with a juvenile-onset neuronal ceroid lipofuscinosis. Electron microscopy of one case showed condensed fingerprint profiles, and genetic analyses identified a novel missense mutation in CLN5. The authors demonstrate the existence of pathogenic CLN5 mutations outside northern Europe and that mutations in this gene can lead to an atypical late-onset neuronal ceroid lipofuscinosis disease, in addition to the late infantile form first described in Finland.

    PMID: 15728307 [PubMed - indexed for MEDLINE]

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