Huntington Disease: Difference between revisions
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'''Original Editor '''- Your name will be added here if you created the original content for this page. | '''Original Editor '''- Your name will be added here if you created the original content for this page. | ||
'''Lead Editors''' | '''Lead Editors''' | ||
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== | == General == | ||
Huntington disease (HD) is an incurable, adult-onset, autosomal dominant inherited disorder which presents with involuntary movements, dementia, and behavioral changes.<br> | |||
== Mechanism of Injury / Pathological Process<br> == | == Mechanism of Injury / Pathological Process<br> == | ||
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References will automatically be added here, see [[Adding References|adding references tutorial]]. | References will automatically be added here, see [[Adding References|adding references tutorial]]. | ||
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Revision as of 23:56, 13 September 2015
Original Editor - Your name will be added here if you created the original content for this page.
Lead Editors
General[edit | edit source]
Huntington disease (HD) is an incurable, adult-onset, autosomal dominant inherited disorder which presents with involuntary movements, dementia, and behavioral changes.
Mechanism of Injury / Pathological Process
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add text here relating to the mechanism of injury and/or pathology of the condition
Clinical Presentation[edit | edit source]
add text here relating to the clinical presentation of the condition
Diagnostic Procedures[edit | edit source]
add text here relating to diagnostic tests for the condition
Outcome Measures[edit | edit source]
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Management / Interventions
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Differential Diagnosis
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Key Evidence[edit | edit source]
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Resources
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Case Studies[edit | edit source]
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Recent Related Research (from Pubmed)[edit | edit source]
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References[edit | edit source]
References will automatically be added here, see adding references tutorial.