Autopsy‐proven Huntington's disease with 29 trinucleotide repeats
Identifieur interne : 001B06 ( Istex/Checkpoint ); précédent : 001B05; suivant : 001B07Autopsy‐proven Huntington's disease with 29 trinucleotide repeats
Auteurs : Christopher Kenney [États-Unis] ; Suzanne Powell [États-Unis] ; Joseph Jankovic [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2007-01.
English descriptors
Abstract
Huntington's disease (HD) is a neurodegenerative disorder associated with expansion of CAG trinucleotide repeats in the huntingtin gene. A minimum of 36 CAG repeats is usually reported in patients with clinical features of HD; 30 to 35 repeats represent an intermediate range. Here we report a 65‐year‐old male with autopsy‐proven HD and 29 CAG repeats. © 2006 Movement Disorder Society
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DOI: 10.1002/mds.21195
Affiliations:
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<author><name sortKey="Powell, Suzanne" sort="Powell, Suzanne" uniqKey="Powell S" first="Suzanne" last="Powell">Suzanne Powell</name>
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<author><name sortKey="Jankovic, Joseph" sort="Jankovic, Joseph" uniqKey="Jankovic J" first="Joseph" last="Jankovic">Joseph Jankovic</name>
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<term>autopsy</term>
<term>chorea</term>
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<term>trinucleotide repeat</term>
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<front><div type="abstract" xml:lang="en">Huntington's disease (HD) is a neurodegenerative disorder associated with expansion of CAG trinucleotide repeats in the huntingtin gene. A minimum of 36 CAG repeats is usually reported in patients with clinical features of HD; 30 to 35 repeats represent an intermediate range. Here we report a 65‐year‐old male with autopsy‐proven HD and 29 CAG repeats. © 2006 Movement Disorder Society</div>
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