Huntington Disease: Difference between revisions
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== General == | == General == | ||
Huntington disease (HD) is an incurable, adult-onset, | Huntington disease (HD) is an incurable, adult-onset, progressive deurodegenerative disorder which presents with involuntary movements, dementia, and behavioral changes<ref>Folstein SE. Huntington's Disease: A Disorder of Families. The Johns Hopkins University Press. 1989</ref>.<br> | ||
HD is named after George Huntington, the physician who described it as hereditary chorea in 1872<ref name="Huntington">Huntington G. On chorea. Med Surg Report. 1872. 26:320</ref>. | HD is named after George Huntington, the physician who described it as hereditary chorea in 1872<ref name="Huntington">Huntington G. On chorea. Med Surg Report. 1872. 26:320</ref>. | ||
== Mechanism of Injury / Pathological Process<br> == | == Mechanism of Injury / Pathological Process<br> == |
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General[edit | edit source]
Huntington disease (HD) is an incurable, adult-onset, progressive deurodegenerative disorder which presents with involuntary movements, dementia, and behavioral changes[1].
HD is named after George Huntington, the physician who described it as hereditary chorea in 1872[2].
Mechanism of Injury / Pathological Process
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Clinical Presentation[edit | edit source]
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Diagnostic Procedures[edit | edit source]
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Outcome Measures[edit | edit source]
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Management / Interventions
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Differential Diagnosis
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Resources
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