Interactive Transcript
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Congenital malformation.
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So we all know Keri two, right? The myelo cyl, Mylo Menil.
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It basically causes a prenatal CSF leak.
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So the tonsils come down,
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but also it affects the, the, uh, cortical folding, um,
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and the migration because you have this essentially
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developmental CSF leak, um, poly micro jia in a,
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in an UNM needed child.
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It can be a little bit hard to diagnose,
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but again, this is a very broad
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and kind of thickened, you know,
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irregular fissure, uh, Sylvie and Fisher.
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And so even if you're not doing a sedated exam, right, just
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to see some of these 2D images to realize that, you know,
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there's something not quite right about this.
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Syl and Fisher, um, holo cephalic, different levels of, uh,
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you know, frontal lobe mal rotation infusion,
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not a subtle diagnosis.
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Uh, tubulopathy, if you see some crazy pan migrational type,
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you know, supinator asymmetric, those are often mutations
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of microtubules because those affect the,
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the actual radial glial fibers along which the neuroglial
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pro genders migrate.
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So again, you know, medical genetics, um, and
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or kind of neuro uh, neurology assessment can be helpful
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for these neuro cutaneous disorders are marked
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by their cutaneous manifestations.
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The surge Weber with this, you know,
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blush over the eyebrow here.
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And so actually this is the normal side, right?
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This is the normally myelinated cortico spinal tract.
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This side is accelerated, right?
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So you have way more myelination T one,
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shortening T two dark than you should in a newborn.
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And you see that there's these dysplastic veins, right?
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So these enhances essentially a venous malformation.
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And so, uh, the brain can't drain in the early stages,
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so it actually has a lot of blood pooling
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and it accelerates myelination.
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It's only later on when those dysplastic, uh, you know,
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cortical veins cannot drain the blood.
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You start to get venous ischemia.
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But in the very early phase, this is actually
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what surge war looks like.
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Tube sclerosis ane was sedation, right?
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So you can have a bunch of tubers,
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which are essentially just migrational anomalies.
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So again, unmyelinated watery brain.
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So you actually have the inverse signal, right?
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It's actually T one bright T two dark.
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Once the patient myelinates, they look the opposite, right?
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They look actually T one dark and T two bright, the tubers.
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But this is what they look like, um, in a neonate.
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And the calcification is really a late finding.
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So usually you only get, uh, a very little,
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a calcification early on.
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Uh, this is a schematic overgrowth,
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so they can have capillary malformations,
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poly dact, poly myco, gy.
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Um, and so this is all pi three ca, um, pathway
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and then nerve continuous melanosis.
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So proliferation of melanocytes in the skin,
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central nervous system.
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Again, this is best done on the neonatal skin
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because as a patient myelinates, these T one deposits start
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to blur with the myelinating brain.