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    Ann Neurol. 2001 Jan;49(1):130-4.

    Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype.

    Illa I, Serrano-Munuera C, Gallardo E, Lasa A, Rojas-García R, Palmer J, Gallano P, Baiget M, Matsuda C, Brown RH.

    Source

    Department of Neurology, Hospital Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Spain. iilla@hsp.santpau.es

    Abstract

    We report a family with a new phenotype of autosomal recessive muscle dystrophy caused by a dysferlin mutation. The onset of the illness is distal, in the muscles of the anterior compartment group. The disease is rapidly progressive, leading to severe proximal weakness. Muscle biopsy showed moderate dystrophic changes with no vacuoles. Dysferlin immunostaining was negative. Gene analysis revealed a frameshift mutation in the exon 50 (delG5966) of the DYSF gene. This phenotype further demonstrates the clinical heterogeneity of the dysferlinopathies.

    PMID:
    11198284
    [PubMed - indexed for MEDLINE]

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