Myopathy as a first symptom of Huntington's disease in a Marathon runner
Identifieur interne : 003C49 ( Main/Merge ); précédent : 003C48; suivant : 003C50Myopathy as a first symptom of Huntington's disease in a Marathon runner
Auteurs : Christoph M. Kosinski [Allemagne] ; Christiane Schlangen [Allemagne] ; Frank N. Gellerich [Allemagne] ; Zemfira Gizatullina [Allemagne] ; Markus Deschauer [Allemagne] ; Johannes Schiefer [Allemagne] ; Anne B. Young [États-Unis] ; Georg Bernhard Landwehrmeyer [Allemagne] ; Klaus V. Toyka [Allemagne] ; Bernd Sellhaus [Allemagne] ; Katrin S. Lindenberg [États-Unis, Allemagne]Source :
- Movement Disorders [ 0885-3185 ] ; 2007-08-15.
English descriptors
- KwdEn :
- Adult, Disease Progression, Humans, Huntington Disease (complications), Huntington Disease (genetics), Male, Mitochondria, Muscle (pathology), Muscle, Skeletal (pathology), Muscular Diseases (etiology), Muscular Diseases (genetics), Muscular Diseases (pathology), Mutation, Oxygen Consumption (physiology), Proton Pumps (genetics), Running, mitochondrial disease, neurodegenerative disease, oxidative stress.
- MESH :
- chemical , genetics : Proton Pumps.
- complications : Huntington Disease.
- etiology : Muscular Diseases.
- genetics : Huntington Disease, Muscular Diseases.
- pathology : Mitochondria, Muscle, Muscle, Skeletal, Muscular Diseases.
- physiology : Oxygen Consumption.
- Adult, Disease Progression, Humans, Male, Mutation, Running.
Abstract
A semi professional marathon runner at risk for Huntington's disease (HD) (43 CAG repeats) developed signs of a slowly progressive myopathy with exercise‐induced muscle fatigue, pain, elevated creatine kinase level, and worsening of his running performance many years before first signs of chorea were detected. Muscle biopsy displayed a mild myopathy with mitochondrial pathology including a complex IV deficiency and analysis of the patient's fibroblast culture demonstrated deficits in mitochondrial function. Challenging skeletal muscle by excessive training might have disclosed myopathy in HD even years before the appearance of other neurological symptoms. © 2007 Movement Disorder Society
Url:
DOI: 10.1002/mds.21550
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<term>Huntington Disease (genetics)</term>
<term>Male</term>
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<front><div type="abstract" xml:lang="en">A semi professional marathon runner at risk for Huntington's disease (HD) (43 CAG repeats) developed signs of a slowly progressive myopathy with exercise‐induced muscle fatigue, pain, elevated creatine kinase level, and worsening of his running performance many years before first signs of chorea were detected. Muscle biopsy displayed a mild myopathy with mitochondrial pathology including a complex IV deficiency and analysis of the patient's fibroblast culture demonstrated deficits in mitochondrial function. Challenging skeletal muscle by excessive training might have disclosed myopathy in HD even years before the appearance of other neurological symptoms. © 2007 Movement Disorder Society</div>
</front>
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<double doi="10.1002/mds.21550"><ISTEX><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Myopathy as a first symptom of Huntington's disease in a Marathon runner</title>
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<title level="j" type="sub">Official Journal of the Movement Disorder Society</title>
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<front><div type="abstract" xml:lang="en">A semi professional marathon runner at risk for Huntington's disease (HD) (43 CAG repeats) developed signs of a slowly progressive myopathy with exercise‐induced muscle fatigue, pain, elevated creatine kinase level, and worsening of his running performance many years before first signs of chorea were detected. Muscle biopsy displayed a mild myopathy with mitochondrial pathology including a complex IV deficiency and analysis of the patient's fibroblast culture demonstrated deficits in mitochondrial function. Challenging skeletal muscle by excessive training might have disclosed myopathy in HD even years before the appearance of other neurological symptoms. © 2007 Movement Disorder Society</div>
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<front><div type="abstract" xml:lang="en">A semi professional marathon runner at risk for Huntington's disease (HD) (43 CAG repeats) developed signs of a slowly progressive myopathy with exercise-induced muscle fatigue, pain, elevated creatine kinase level, and worsening of his running performance many years before first signs of chorea were detected. Muscle biopsy displayed a mild myopathy with mitochondrial pathology including a complex IV deficiency and analysis of the patient's fibroblast culture demonstrated deficits in mitochondrial function. Challenging skeletal muscle by excessive training might have disclosed myopathy in HD even years before the appearance of other neurological symptoms.</div>
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