Huntington's disease classification: Difference between revisions
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{{Huntington's disease}} | {{Huntington's disease}} | ||
{{CMG}} {{AE}} {{SAH}} | |||
==Overview== | |||
==Classification== | |||
*There are two forms of Huntington's disease. The most common is adult-onset Huntington's disease. Persons with this form usually develop symptoms in their mid 30s and 40s. | |||
*An early-onset form of Huntington's disease accounts for a small number of cases and begins in childhood or adolescence. Symptoms may resemble those of Parkinson's disease with rigidity, slow movements, and [[Essential tremor(patient information)|tremor]]. | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
Latest revision as of 14:51, 25 October 2018
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Huntington's disease Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Huntington's disease classification On the Web |
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American Roentgen Ray Society Images of Huntington's disease classification |
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Risk calculators and risk factors for Huntington's disease classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Syed Ahsan Hussain, M.D.[2]
Overview
Classification
- There are two forms of Huntington's disease. The most common is adult-onset Huntington's disease. Persons with this form usually develop symptoms in their mid 30s and 40s.
- An early-onset form of Huntington's disease accounts for a small number of cases and begins in childhood or adolescence. Symptoms may resemble those of Parkinson's disease with rigidity, slow movements, and tremor.