Interactive Transcript
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I have a FLAIR image up of our patient
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with Huntington's Chorea.
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A little bit of quick anatomy.
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The inner and outer aspect of the globus pallidus,
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known as GPI and GPE.
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Then the putamen divided up into two.
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We'll see it a little bit later on.
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There's an inner and outer aspect of the putamen.
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Then the external capsule, then the gray matter,
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claustrom, then the extreme capsule,
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this white stripe,
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and then the centrosylvian cortex.
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I want to briefly take a moment and talk about
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some other metabolic causes of Chorea.
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One of these is hyperthyroidism.
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Now, there's a common theme here.
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Hyperthyroidism drives the mitochondria to produce
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more energy, produce, produce, produce.
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It's basically using its thyroid hormone
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whip against the mitochondria.
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So it's not a coincidence that people with
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Huntington's Chorea develop toxicity at the
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mitochondrial level.
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This is also true for people that have ballism,
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which is a subset of Chorea.
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So this can happen as a manifestation
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of thyrotoxicosis.
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This can also happen as a manifestation
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of hyperglycemia,
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as we discussed in an earlier vignette,
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when you correct the thyrotoxicosis or correct
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the hyperglycemia, the patients get better,
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unless they have prior risk factors for Chorea.
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So, it's very important to know what the patient's
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past medical history consists of.
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There's one other entity that may be associated
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with chorea and also dystonia,
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and that's Wilson's disease.
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It is not a coincidence that this
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is an abnormality of copper.
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And where do you need copper?
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For the oxidative phosphorylative pathway.
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And where is that utilized?
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In the mitochondria.
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So there is a common theme here.
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Mitochondrial toxicity, mitochondrial destruction,
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mitochondrial poisoning in these
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metabolic syndromes.
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Not unlike what occurs in the
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CAG, cytosine adenine guanine repeats
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that produce Huntington's Chorea.
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