Movement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studies
Identifieur interne : 001E78 ( Istex/Curation ); précédent : 001E77; suivant : 001E79Movement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studies
Auteurs : Truong [Royaume-Uni, États-Unis] ; Harding [Royaume-Uni] ; F. Scaravilli [Royaume-Uni] ; S. J. M. Smith [Royaume-Uni] ; J. A. Morgan-Hughes [Royaume-Uni] ; C. D. Marsden [Royaume-Uni]Source :
- Movement Disorders [ 0885-3185 ] ; 1990.
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Abstract
Of 85 consecutive patients with mitochondrial myopathy, 29 had clinically significant central nervous system involvement. Nine of these had movement disorders that included dystonia, chorea, parkinsonism, and myoclonus. Autopsy studies of one patient with ataxia, dementia, and parkinsonism followed by dystonia showed the features of olivopontocerebellar atrophy with additional degenerative changes in the basal ganglia. Postmortem in a further case with myoclonus, deafness, muscle weakness, retinopathy, and ataxia showed symmetrical mineralisation of the striatopallidodentatal system.
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DOI: 10.1002/mds.870050204
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Marsden</name><affiliation wicri:level="2"><mods:affiliation>University Department of Clinical Neurology, National Hospital for Nervous Diseases, Queen Square, London, England</mods:affiliation><country>Royaume-Uni</country><placeName><region type="country">Angleterre</region></placeName><wicri:cityArea>University Department of Clinical Neurology, National Hospital for Nervous Diseases, Queen Square, London</wicri:cityArea></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</title><title level="j" type="sub">Official Journal of the Movement Disorder Society</title><title level="j" type="abbrev">Mov. Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="1990">1990</date><biblScope unit="vol">5</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="109">109</biblScope><biblScope unit="page" to="117">117</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">B0CC46C895A1BB0FDB2DF5D5860288D7D39258F1</idno><idno type="DOI">10.1002/mds.870050204</idno><idno type="ArticleID">MDS870050204</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Chorea</term><term>Dystonia</term><term>Mitochondrial myopathy</term><term>Myoclonus</term><term>Olivopontocerebellar atrophy</term><term>Striatonigral degeneration</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Of 85 consecutive patients with mitochondrial myopathy, 29 had clinically significant central nervous system involvement. Nine of these had movement disorders that included dystonia, chorea, parkinsonism, and myoclonus. Autopsy studies of one patient with ataxia, dementia, and parkinsonism followed by dystonia showed the features of olivopontocerebellar atrophy with additional degenerative changes in the basal ganglia. Postmortem in a further case with myoclonus, deafness, muscle weakness, retinopathy, and ataxia showed symmetrical mineralisation of the striatopallidodentatal system.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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