Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/11257
Title: Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6.
Authors: Arsov, Todor;Smith, Katherine R;Damiano, John Anthony;Franceschetti, Silvana;Canafoglia, Laura;Bromhead, Catherine J;Andermann, Eva;Vears, Danya F;Cossette, Patrick;Rajagopalan, Sulekha;McDougall, Alan;Sofia, Vito;Farrell, Michael;Aguglia, Umberto;Zini, Andrea;Meletti, Stefano;Morbin, Michela;Mullen, Saul A;Andermann, Frederick;Mole, Sara E;Bahlo, Melanie;Berkovic, Samuel F
Affiliation: Epilepsy Research Center, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria 3084, Australia.
Issue Date: 5-May-2011
Citation: American Journal of Human Genetics 2011; 88(5): 566-73
Abstract: The molecular basis of Kufs disease is unknown, whereas a series of genes accounting for most of the childhood-onset forms of neuronal ceroid lipofuscinosis (NCL) have been identified. Diagnosis of Kufs disease is difficult because the characteristic lipopigment is largely confined to neurons and can require a brain biopsy or autopsy for final diagnosis. We mapped four families with Kufs disease for whom there was good evidence of autosomal-recessive inheritance and found two peaks on chromosome 15. Three of the families were affected by Kufs type A disease and presented with progressive myoclonus epilepsy, and one was affected by type B (presenting with dementia and motor system dysfunction). Sequencing of a candidate gene in one peak shared by all four families identified no mutations, but sequencing of CLN6, found in the second peak and shared by only the three families affected by Kufs type A disease, revealed pathogenic mutations in all three families. We subsequently sequenced CLN6 in eight other families, three of which were affected by recessive Kufs type A disease. Mutations in both CLN6 alleles were found in the three type A cases and in one family affected by unclassified Kufs disease. Mutations in CLN6 are the major cause of recessive Kufs type A disease. The phenotypic differences between variant late-infantile NCL, previously found to be caused by CLN6, and Kufs type A disease are striking; there is a much later age at onset and lack of visual involvement in the latter. Sequencing of CLN6 will provide a simple diagnostic strategy in this disorder, in which definitive identification usually requires invasive biopsy.
Internal ID Number: 21549341
URI: http://ahro.austin.org.au/austinjspui/handle/1/11257
DOI: 10.1016/j.ajhg.2011.04.004
URL: http://www.ncbi.nlm.nih.gov/pubmed/21549341
Type: Journal Article
Subjects: Adolescent
Adult
Age of Onset
Biopsy
Dementia.pathology
Exons
Female
Genetic Linkage
Genetic Testing.methods
Genotype
Heterozygote
Humans
Male
Membrane Proteins.genetics
Middle Aged
Mutation
Neuronal Ceroid-Lipofuscinoses.etiology.genetics
Pedigree
Polymorphism, Single Nucleotide
Appears in Collections:Journal articles

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