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Localisation of merosin-positive congenital muscular dystrophy to chromosome 4p16.3
Authors:G S Sellick  C Longman  M Brockington  I Mahjneh  L Sagi  K Bushby  H Topalo?lu  F Muntoni  R S Houlston
Institution:(1) Section of Cancer Genetics, Institute of Cancer Research, 15 Cotswold Rd, Sutton, Surrey, UK;(2) Department of Paediatrics, Imperial College, Hammersmith Hospital, London, UK;(3) Department of Medical Genetics, Yorkhill Hospital, Glasgow, UK;(4) University of Oulu and Pietarsaari Hospital, Pietarsaari, Finland;(5) Institute of Human Genetics, University Newcastle upon Tyne, Newcastle, UK;(6) Department of Paediatric Neurology, Hacettepe Childrenrsquos Hospital, Ankara, Turkey
Abstract:The congenital muscular dystrophies (CMD) are a heterogeneous group of autosomal recessive disorders, which present within the first 6 months of life with hypotonia, muscle weakness and contractures, associated with dystrophic changes on skeletal muscle biopsy. We have previously reported a large consanguineous family segregating merosin-positive congenital muscular dystrophy, in which involvement of known CMD loci was excluded. A genome-wide linkage search of the family conducted using microsatellite markers spaced at 10-Mb intervals failed to identify a disease locus. A second scan using a high-density SNP array, however, permitted a novel CMD locus on 4p16.3 to be identified (multipoint LOD score 3.4). Four additional consanguineous CMD families with a similar phenotype were evaluated for linkage to a 4.14-Mb interval on 4p16.3; however, none showed any evidence of linkage to the region. Our findings further illustrate the utility of highly informative SNP arrays compared with standard panels of microsatellite markers for the mapping of recessive disease loci.
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